Alvizia Healthcare Private Limited
Alvizia Healthcare Private Limited
Sector 38-C, Chandigarh
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Pharma Tablets


Leading Manufacturer and Trader of Pharma Tablets such as Atmofin Forte Tablet, Atmofix 100mg 200mg Tablet, Atmofix Cl 325 Mg Tablet, Atmofix Oz Tablets, Atmoflox 200mg Tablet, Atmoflex Gm Tablet and many more items from Chandigarh.

Approx. Rs 15 / Pack
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Cefuroxime is a B-lactam type antibiotic. More specifically, it is a second-generation cephalosporin. Cephalosporins work the same way as penicillins: they interfere with the peptidoglycan synthesis of the bacterial wall by inhibiting the final transpeptidation needed for the cross-links. This effect is bactericidal. Cefuroxime is effective against the following organisms: Aerobic Gram-positive Microorganisms: Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes. Aerobic Gram-negative Microorganisms: Escherichia coli, Haemophilus influenzae (including beta-lactamase-producing strains), Haemophilus parainfluenzae, Klebsiella pneumoniae, Moraxella catarrhalis (including beta-lactamase-producing strains), Neisseria gonorrhoeae (including beta-lactamase-producing strains). Spirochetes: Borrelia burgdorferi. Cefuroxime axetil is the prodrug.

Composition:

  • Cefuroxime Axetil IP 250 mg/500 mg

Packing:

  • 1x4
  • 10x1x4 (Alu-Alu)

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Approx. Rs 119 / Pack(s)
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Mechanism of Action Fexofenadine: Like other H1-blockers, Fexofenadine competes with free histamine for binding at H1-receptors in the GI tract, large blood vessels, and bronchial smooth muscle. This block the action of endogenous histamine, which subsequently leads to temporary relief of the negative symptoms (eg. nasal congestion, watery eyes) brought on by histamine. Fexofenadine exhibits no anticholinergic, antidopaminergic, alpha1-adrenergic or beta-adrenergic-receptor blocking effects.
Montelukast selectively antagonizes leukotriene D4 (LTD4) at the cysteinyl leukotriene receptor, CysLT1, in the human airway. Montelukast inhibits the actions of LTD4 at the CysLT1 receptor, preventing airway edema, smooth muscle contraction, and enhanced secretion of thick, viscous mucus.

Composition:
  • Fexofenadine Hydrochloride IP 120 mg
  • Montelukast Sodium IP 10 mg

Packing:

  • 1x1010x1x10(Alu-Alu)

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Approx. Rs 72 / Pack(s)
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Mechanism of Action:

  • Azithromycin is a macrolide antibacterial drug. Azithromycin concentrates in phagocytes and fibroblasts as demonstrated byin vitro incubation techniques. Using such methodology, the ratio ofintracellular to extracellular concentration was > 30 after one hour of incubation. In vivo studies suggest that concentration in phagocytes may contribute to drug distribution to inflamed tissues.

Composition:

  • Azithromycin Dihydrate IP 250 mg/500 mg

Packing:


  • 1x3
  • 10x1x3
  • (Blister)


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    Approx. Rs 38 / Piece(s)
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    Cinnarizine is an antihistamine and a calcium channel blocker. Histamines mediate a number of activities such as contraction of smooth muscle of the airways and gastrointestinal tract, vasodilatation, cardiac stimulation, secretion of gastric acid, promotion of interleukin release and chemotaxis of eosinophils and mast cells. Competitive antagonists at histamine H1 receptors may be divided into first (sedating) and second (non-sedating) generation agents. Some, such as Cinnarizine also block muscarinic acetylcholine receptors and are used as anti-emetic agents. Cinnarizine through its calcium channel blocking ability also inhibits stimulation of the vestibular system.

    Composition:

    • Each Uncoated Tablet Contains
    • Cinnarizine IP 25 mg/75 mg

    Packing: 10x10(Blister)

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    Approx. Rs 57 / Pack(s)
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    Being a well established organization, we bring forward an excellent quality range of Atmoflox 200mg Tablet. This tablet is highly active against enterobacteriaceae, Haemophilus influenzae, Streptococcus pyogens & Streptococcus pneumonia & many beta lactamase producing bacteria. Our offered tablet is highly acknowledged among our prestigious clients for its effectiveness. This tablet is precisely processed using supreme grade chemical compounds and modern technology under the direction of deft professionals.

    Features:

    • Effectiveness
    • Safe to consume
    • Quick results

    Mechanism of Action:

    • Ofloxacin is a quinolone carboxylic acid derivative which has a broad spectrum of antibacterial activity against both Gram-positive and Gram-negative bacteria. Ofloxacin exerts its effect by inhibiting the bacterial DNA gyrase, which is responsible for coiling the genetic material as a prerequisite for bacterial multiplication.The mode of action, range of activities, duration of action and MIC levels have been established mainly by means of in vitro studies using bacterial isolates. Ofloxacin is readily absorbed and excreted mainly unchanged in the urine. The serum elimination half-life is approximately 6 to 8 hours.
    • Following oral administration, ofloxacin peak serum concentrations are reached within one to two hours. The plasma level usually achieved by the recommended dosage regimens (3 to 4 micrograms/mL) is in excess of the average MIC which is 1 to 2 micrograms/mL, for susceptible organisms. Ofloxacin has a low (9,4%) plasma protein binding. Ofloxacin has a bactericidal effect. In vitro tests show that strains in which the sensitivity varies include pneumococci and ureaplasma urealyticum.

    Strains that are normally resistant are:

    • Peptococcus, Peptostreptococcus, Eubacterium spp., Fusobacterium spp. and Treponema pallidum.

    Composition Each Film coated Tablet Contains:

    • Ofloxacin IP 200 mg

    Packing:

    • 10x10 (Alu-Alu)

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    Approx. Rs 168 / Pack(s)
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    We are a well-renowned organization in the industry to provide our patrons the best quality array of Atmofix Oz Tablets. Under the stern guidance of deft workforce, the offered tablet is well-processed using optimum class chemical compounds and sophisticated technology in tandem with the set medical industry norms. Moreover, this tablet is precisely tested against several parameters of quality to avoid any kind of impurity. The provided tablet is used to treat a wide variety of bacterial infections.

    Features:

    • Free from side effects
    • Proper composition
    • Hygienically processed

    Composition:


    • Cefixime 200 mg, Ornidazole 500 mg

    Packing
    • 10X1X10


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    Approx. Rs 69 / Pack
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    Being a customer oriented organization, we are highly engaged in offering a wide range of Atmofin Forte Tablet that is processed making use of premium class chemical compounds and advanced processing technology under the strict supervision of adroit professionals. In synchronization with set medical industry standards, this tablet is carefully examined on diverse measures of quality. Apart from this, provided tablet is used to treat bacterial infections.

    Features:

    • Safe usage
    • Long shelf life
    • Effectiveness

    Composition:


    • Diclofenac Potassium BP 50 mg
    • Paracetamol IP 325 mg
    • Serratiopeptidase IP 10 mg

    Packing:

    • 10x2x10(Blister)

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    Approx. Rs 235 / Pack(s)
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    Mechanism of Action:

    • This is a semisynthetic (partially manmade), oral antibiotic in the cephalosporin family of antibiotics and it stops bacteria from multiplying by preventing bacteria from forming the walls that surround them. The walls are necessary to protect bacteria from their environment and to keep the contents of the bacterial cell together so without a cell wall bacteria cannot survive and die and Clavulanic acid is a naturally derived beta lactamase inhibitor produced by Streptomyces clavuligerus. Clavulanic acid is an irreversible inhibitor of intracellular and extracellular Beta-lactamases, demonstrating concentration-dependent and competitive inhibition.

    Composition Each Tablet Contains:

    • Cefixime Trihydrate IP 200 mg
    • Clavulanic acid 125 mg

    Packing:

    • 10X10 (Alu-Alu)

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    Approx. Rs 180 / Pack(s)
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    Composition Each Film Coated Tablet Contains:

    • Glucosamine Sulphate 500 mg
    • Methyl Sulphonyl Methane 50 mg
    • Diacerein 50 mg and Excipients Q.S

    Packing:

    • 5X3X10(Alu Alu)

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    Approx. Rs 95 / Pack(s)
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    Composition Each Film Coated Tablet Contains:

    • Ofloxacin IP 200 mg
    • Ornidazole IP 500 mg

    Packing:

    • 10x1x10(Blister)

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    Approx. Rs 17 / Pack
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    Composition Each Uncoated Tablet Contains:

    • Fluconazole IP 150 mg

    Packing:

    • 30x1 (Blister)

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    Approx. Rs 130 / Pack(s)
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    Composition:
    • Each Film Coated Tablet Contains:
    • Cefuroxime Axetil IP 250 mg/500 mg

    Packing:

    • 10x1x6 (Alu-Alu)


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      Approx. Rs 248 / Piece(s)
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      Composition:
      • Cefuroxime Axetil IP 500 mg
      • Clavulanic Acid 125 mg

      Packing:


      • 10x1x6(Alu Alu)

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      Approx. Rs 119 / Pack(s)
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      BEFORE TAKING THIS MEDICINE TELL THE DOCTOR ABOUT ANY MEDICAL PROBLEMS AN ALLERGIES THAT CHILD HAS NOW OR HAS HAD. Some medicines may affect how patient's works, or other medicine work. If anyone is taking or has recently taken other medicines, including those obtained without a prescription.

      Composition:
      • Levocetirizine Hydrochloride IP 5 mg
      • Montelukast Sodium IP 10 mg

      Packing:

      • 10x10 (Alu-Alu)



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      Approx. Rs 299 / Pack(s)
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      Mechanism of Action:

      • Linezolid is a synthetic antibacterial agent. It inhibits bacterial protein synthesis by binding to bacterial 23S ribosomal RNA of the 50S subunit. This prevents the formation of a functional 70S initiation complex that is essential for the bacterial translation process. Linezolid is bacteriostatic against enterococci and staphylococci and bactericidal against most strains of streptococci.

      Composition:

      • Each Tablet Contains:
      • Linezolid 600 mg

      Packing:
      • 10x1x4(Alu-Alu)

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      Approx. Rs 58 / Pack(s)
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      Rabeprazole belongs to a class of antisecretory compounds (substituted benzimidazole proton-pump inhibitors) that do not exhibit anticholinergic orhistamine H2- receptor antagonist properties, but suppress gastric acid secretion by inhibiting the gastric H+, K+ATPase at the secretory surface of the gastric parietal cell. Because this enzyme is regarded as the acid (proton) pump within the parietal cell, rabeprazole has been characterized as a gastric proton-pump inhibitor. Rabeprazole blocks the final step of gastric acid secretion.
      In gastric parietal cells, rabeprazole is protonated, accumulates, and is transformed to an active sulfenamide. When studied in vitro, rabeprazole is chemically activated at pH 1.2 with a half-life of 78 seconds. It inhibits acid transport in porcine gastric vesicles with a half-life of 90 seconds.

      Composition:
      • Rabeprazole Sodium IP 20 mg

      Packing:
      • 10x10(Alu-Alu)



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      Approx. Rs 68 / Pack(s)
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      Rabeprazole sodium suppresses gastric acid secretion by the specific inhibition of the H+/K+-ATPase enzyme (proton pump) at the secretory surface of the gastric parietal cell thereby blocking the final step of acid production. This effect is dose-related and leads to inhibition of both basal and stimulated acid secretion irrespective of the stimulus. Domperidone is a dopamine antagonist (it acts by antagonizing the D2 receptor) with anti-emetic properties. It does not cross the blood brain barrier. Its anti-emetic effect may be due to a combination of peripheral (gastrokinetic) effects and antagonism of dopamine receptors in the chemoreceptor trigger zone, which lies outside the blood-brain barrier in the area postrema. Studies in man have shown oral domperidone to increase lower oesophageal pressure, improve antroduodenal motility and accelerate gastric emptying. There is no effect on gastric secretion. Domperidone is a dopamine antagonist with antiemetic properties. Domperidone does not readily cross the blood-brain barrier. Its antiemetic effect may be due to a combination of peripheral (gastrokinetic) effects and antagonism of central dopamine receptors in the chemoreceptor trigger zone which lies in the area postrema and is regarded as being outside the blood-brain barrier.

      Composition:
      • Rabeprazole 20 mg and Domperidone 10 mg

      Packing:

      • 10x10 (Alu-Alu)

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      Approx. Rs 185 / Pack(s)
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      Tranexamic acid (AMCA) is a potent antifibrinolytic drug occurring in two isomeric forms; the antifibrinolytic potency resides in the transisomeric form. The main action of AMCA is blocking of the lysine-binding sites of the plasminogen molecule, which are of importance for the binding to fibrin. This prevents activation of plasminogen by plasminogen activator also absorbed to fibrin. AMCA can be administered perorally or intravenously and is excreted into the urine. It enters tissues and fluids in various concentrations and crosses the placenta. There is no evidence of a thrombogenic effect of AMCA, but in accordance with its action, it prolongs dissolution of fibrin deposits already formed. AMCA is a drug of high clinical value for the treatment of bleedings due to both systemic and local fibrinolysis Ponstel (mefenamic acid) is a non-steroidal anti-inflammatory drug (NSAID) that exhibits anti-inflammatory, analgesic, and antipyretic activities in animal models.

      Composition:

      • Tranexamic Acid 500 mg and Mefenamic Acid 250 mg


      Packing:

      • 10x10(Alu-Alu)


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      Approx. Rs 68 / Pack
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      Lornoxicam inhibits prostaglandin biosynthesis by blocking the enzyme Cyclo- oxygenase. Lornoxicam inhibits both isoforms in the same concentration range, that is, Balanced COX-1 Inhibition & COX-2 inhibition through that it's a safest pain killer. It is distinguished from established oxicams by a relatively short elimination half-life (3 to 5 hours), which may be advantageous from a tolerability standpoint. The absolute bioavailability of Lornoxicam is 90-100% and no first pass effect was observed.
      Paracetamol is usually classified along with nonsteroidal anti-inflammatory drugs (NSAID), Like all drugs of this class, its main mechanism of action is the inhibition of Cyclo oxygenase (COX). Paracetamol is a p-aminophenol derivative that exhibits analgesic and antipyretic activity. It does not possess anti-inflammatory activity. Paracetamol is thought to produce analgesia through a central inhibition of prostaglandin synthesis.

      Composition:

      • Lornoxicam IP 8 mg
      • Paracetamol IP 325 mg


      Packing:

      • 10x10(Alu-Alu)

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      Approx. Rs 135 / Pack(s)
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      Composition:


      • Lornoxicam IP 8 mg
      • Thiocolchicoside IP 4 mg

      Packing:

      • 10x10(Alu Alu)


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      Approx. Rs 72 / Pack(s)
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      Mechanism of Action:

      • Azithromycin is a macrolide antibacterial drug. Azithromycin concentrates in phagocytes and fibroblasts as demonstrated byin vitro incubation techniques. Using such methodology, the ratio ofintracellular to extracellular concentration was > 30 after one hour of incubation. In vivo studies suggest that concentration in phagocytes may contribute to drug distribution to inflamed tissues.

      Composition:

      • Azithromycin Dihydrate IP 250 mg/500 mg

      Packing:

      • 1x6
      • 10x1x6 (Blister)


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      Approx. Rs 176 / Pack(s)
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      Composition:

      Cefixime Trihydrate IP 200 mg
      Azithromycin Dihydrate IP 250 mg

      Packing:

      • 10x1x10(Alu Alu)

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      Approx. Rs 96 / Pack(s)
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      Azithromycin acts by binding to the 50S ribosomal subunit of susceptible microorganisms and, thus, interfering with microbial protein synthesis. Nucleic acid synthesis is not affected. Azithromycin concentrates in phagocytes and fibroblasts as demonstrated by in vitro incubation techniques. Fluconazole is a highly selective inhibitor of fungal cytochrome P450 sterol C-14-a-demethylation. Mammalian cell demethylation is much less sensitive to fluconazole inhibition. The subsequent loss of normal sterols correlates with the accumulation of 14-a-methyl sterols in fungi and may be responsible for the fungistatic activity of fluconazole.Secnidazole is the first nitroimidazole to offer a 3-day antiprotozoal activity from one single dose. With its prolonged half life, (secnidazole) offers an effective treatment and thus ensures improved patient compliance because of the short duration of treatment with excellent therapeutic efficacy.

      Composition:

      • A. One Fluconazole Tablet IP 150 mg
      • Each uncoated tablet contains
      • Fluconazole IP 150 mg
      • B. One Azithromycin Tablet IP 1g
      • Each film Coated tablet contains
      • Azithromycin Dihydrate IP
      • eq. to Azithromycin 1 g
      • C. Two Secnidazole Tablets IP 1g
      • Each film coated tablet contains
      • Secnidazole IP 1 g

      Packing:

      • 10X1X4(Blister)

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      Approx. Rs 62 / Piece(s)
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      Cinnarizine is an antihistamine and a calcium channel blocker. Histamines mediate a number of activities such as contraction of smooth muscle of the airways and gastrointestinal tract, vasodilatation, cardiac stimulation, secretion of gastric acid, promotion of interleukin release and chemotaxis of eosinophils and mast cells. Competitive antagonists at histamine H1 receptors may be divided into first (sedating) and second (non-sedating) generation agents. Some, such as Cinnarizine also block muscarinic acetylcholine receptors and are used as anti-emetic agents. Cinnarizine through its calcium channel blocking ability also inhibits stimulation of the vestibular system.

      Composition:

      • Each Uncoated Tablet Contains:
      • Cinnarizine IP 25 mg/75 mg

      Packing:

      • 10x10(Alu-Alu)

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      Approx. Rs 45 / Pack(s)
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      Cinnarizine has Ca channel blocking activity selective for arterial smooth muscles. It has some antihistamine activity. Cinnarizine acts as a labyrinthine
      . It also improves microcirculation by reducing ischaemia-induced blood viscosity. Domperidone is a peripheral dopamine-receptor blocker. It increases both the oesophageal peristalsis and the lower oesophageal sphincter pressure. It also increases gastric motility and peristalsis, and enhances gastroduodenal coordination, thus facilitating gastric emptying and decreasing small bowel transit time.

      Composition:
      • Cinnarizine IP 20 mg and Domperidone Maleate IP 15 mg

      Packing:


      • 10x10(Alu-Alu)

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      Approx. Rs 62 / Piece(s)
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      Cinnarizine is an antihistamine and a calcium channel blocker. Histamines mediate a number of activities such as contraction of smooth muscle of the airways and gastrointestinal tract, vasodilatation, cardiac stimulation, secretion of gastric acid, promotion of interleukin release and chemotaxis of eosinophils and mast cells. Competitive antagonists at histamine H1 receptors may be divided into first (sedating) and second (non-sedating) generation agents. Some, such as Cinnarizine also block muscarinic acetylcholine receptors and are used as anti-emetic agents. Cinnarizine through its calcium channel blocking ability also inhibits stimulation of the vestibular system.

      Composition:

      • Each Uncoated Tablet Contains
      • Cinnarizine IP 25 mg/75 mg

      Packing: 10x10(Alu-Alu)

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      Approx. Rs 20 / Pack
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      Other Details:

      • Etodolac 300mg, Paracetamol 325 mg

      Packing:

      • 10x1x10

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      Approx. Rs 170 / Pack(s)
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      Mechanism of Action:

      • After combination of Etoricoxib and Thiocolchicoside we observed that Etoricoxib is selective inhibitor of COX-2 that decreases GI toxicity and is without effects on platelet function. Thiocolchicoside, is a muscle relaxant, which has been claimed to possess GABA (gamma-Aminobutyric acid) mimetic and glycinergic actions. It is used in the symptomatic treatment of painful muscle spasm.
      • It has been demonstrated by recent studies concomitant administration of an Etoricoxib and Thiocolchicoside shows significantly better symptoms relief compared with the modest improvement of inflammation with each of the treatment alone.

      Composition:

      • Etoricoxib IP 60 mg
      • Thiocolchicoside IP 4 mg

      Packing:

      • 1x10
      • 10x1x10 (Alu-Alu)

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      Approx. Rs 295 / Pack(s)
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      Mechanism of Action:

      • After combination of Etoricoxib and Thiocolchicoside we observed that Etoricoxib is selective inhibitor of COX-2 that decreases GI toxicity and is without effects on platelet function. Thiocolchicoside, is a muscle relaxant, which has been claimed to possess GABA (gamma-Aminobutyric acid) mimetic and glycinergic actions. It is used in the symptomatic treatment of painful muscle spasm.
      • It has been demonstrated by recent studies concomitant administration of an Etoricoxib and Thiocolchicoside shows significantly better symptoms relief compared with the modest improvement of inflammation with each of the treatment alone.

      Composition:
      • Etoricoxib IP 60 mg
      • Thiocolchicoside IP 8 mg

      Packing:

      • 1x10
      • 10x1x10
      • (Alu-Alu)

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        Approx. Rs 120 / Pack(s)
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        Gabapentin [1-(aminomethyl)cyclohexane acetic acid] is a novel anti-epileptic agent, originally developed as a gamma-aminobutyric acid (GABA)-mimetic compound to treat spasticity, and has been shown to have potent anticonvulsive effects. Initially approved only for use in partial seizures, it soon showed promise in the treatment of chronic pain syndromes, especially neuro-pathic pain.

        Composition:

        • Gabapentin USP 300 mg
        • Methylcobalamin JP 500 mcg

        Packing:

        • 10x10(Alu-Alu)


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        Approx. Rs 495 / Pack(s)
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        Composition:
        • A: 1 Mifepristone Tablet IP
        • Each uncoated tablet contains
        • Mifepristone IP 200 mg
        • B: 4 Misoprostol Tablets IP
        • Each uncoated tablet contains
        • Misoprostol IP 200 mcg
        • (As Misoprostol 1% Dispersion)

        Packing:

        • 1 Kit 10 x 1 Kit (Alu-Alu)


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        Approx. Rs 38 / Pack
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        Nimesulide is rapidly absorbed following oral administration. Food, gender and advanced age have negligible effects on Nimesulide pharmacokinetics. The protein binding of Nimesulide is >97.5%. Nimesulide posses a shorter half life (1.8-4.7) and is hepatically metabolized. 50% of the drug is renally eliminated.

        Composition:
        • Nimesulide BP 100 mg
        • Paracetamol IP 325 mg
        Packing:

        • 10x10(Blister)

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        Approx. Rs 29 / Pack(s)
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        Nimesulide is fairly rapidly absorbed from the gastrointestinal tract. The volume of distribution in the post distribution phase for Nimesulide ranges from 0.19 to 0.39 L/kg, indicating that the drug is principally distributed in the extra cellular fluid compartment. Nimesulide is almost exclusively metabolized and cleared by the liver. After oral administration of Nimesulide 100 mg, the apparent mean elimination half-life (t½β) varied from 1.96 to 4.75 hours. Nimesulide is mainly eliminated by the renal route.

        Composition:

        • Nimesulide BP 100 mg

        Packing:
        • 4x5x10(Blister)


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        Alvizia Healthcare Private Limited
        Anjum Aggarwal  (Managing Director)
        SCO 165, Ground Floor, Sector 38-C
        Chandigarh - 160036 , India
        Send E-mail