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Product NDC Code | 70771-1084 | ||||
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Drug Name | Mycophenolate mofetil |
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Type | Generic | ||||
Pharm Class | Antimetabolite Immunosuppressant [EPC] | ||||
Active Ingredients |
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Route | INTRAVENOUS | ||||
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION | ||||
RxCUI drug identifier | 311881 | ||||
Application Number | ANDA204473 | ||||
Labeler Name | Zydus Lifesciences Limited | ||||
Packages |
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Check if available Online | Get Medication Prices online with Discount |
Spl product data elements
Usually a list of ingredients in a drug product.Mycophenolate Mofetil Mycophenolate Mofetil MYCOPHENOLATE MOFETIL MYCOPHENOLIC ACID POLYSORBATE 80 ANHYDROUS CITRIC ACID WATER HYDROCHLORIC ACID SODIUM HYDROXIDE
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.PACKAGE LABEL.PRINCIPAL DISPLAY PANEL PRINCIPAL DISPLAY PANEL – MYCOPHENOLATE MOFETIL 500 MG CONTAINER LABEL NDC 70771-1084-1 Mycophenolate Mofetil for Injection, USP (500 mg per Vial) FOR INTRAVENOUS INFUSION ONLY PHARMACIST: Dispense the Medication Guide provided separately to each patient. SINGLE DOSE VIAL Rx only Zydus Pharmaceuticals PRINCIPAL DISPLAY PANEL - MYCOPHENOLATE MOFETIL 500 MG CARTON LABEL NDC 70771-1084-8 Mycophenolate Mofetil for Injection, USP (500 mg per Vial) PHARMACIST: Dispense the Medication Guide provided separately to each patient. FOR INTRAVENOUS INFUSION ONLY SINGLE DOSE VIAL 4 Vials Rx only Zydus Pharmaceuticals Container Label Carton Label
Spl medguide
Information about the patient medication guide that accompanies the drug product. Certain drugs must be dispensed with an accompanying medication guide. This field may contain information about when to consult the medication guide and the contents of the medication guide.SPL MEDGUIDE
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API