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Product NDC Code | 70771-1702 | ||||||||||||
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Drug Name | Famotidine |
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Type | Generic | ||||||||||||
Pharm Class | Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC] |
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Active Ingredients |
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Route | ORAL | ||||||||||||
Dosage Form | TABLET, FILM COATED | ||||||||||||
RxCUI drug identifier | 284245, 310273 |
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Application Number | ANDA216441 | ||||||||||||
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.Famotidine Famotidine FAMOTIDINE FAMOTIDINE HYPROMELLOSE 2910 (5 MPA.S) HYPROMELLOSE 2910 (6 MPA.S) MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE 101 MICROCRYSTALLINE CELLULOSE 102 POLYETHYLENE GLYCOL 8000 SILICON DIOXIDE SODIUM STARCH GLYCOLATE TYPE A STARCH, CORN TALC TITANIUM DIOXIDE off white Z21 Famotidine Famotidine FAMOTIDINE FAMOTIDINE HYPROMELLOSE 2910 (5 MPA.S) HYPROMELLOSE 2910 (6 MPA.S) MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE 101 MICROCRYSTALLINE CELLULOSE 102 POLYETHYLENE GLYCOL 8000 SILICON DIOXIDE SODIUM STARCH GLYCOLATE TYPE A STARCH, CORN TALC TITANIUM DIOXIDE off white Z41
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 NDC 70771-1702-3 Famotidine Tablets USP, 20 mg 30 Tablets Rx only NDC 70771-1703-3 Famotidine Tablets USP, 40 mg 30 Tablets Rx only 20 mg label 40 mg label
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