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Famotidine - Medication Information

Product NDC Code 70771-1703
Drug Name

Famotidine

Type Generic
Pharm Class Histamine H2 Receptor Antagonists [MoA],
Histamine-2 Receptor Antagonist [EPC]
Active Ingredients
Famotidine 40 mg/1
Route ORAL
Dosage Form TABLET, FILM COATED
RxCUI drug identifier 284245,
310273
Application Number ANDA216441
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1703-0 1000 tablet, film coated in 1 bottle (70771-1703-0)
70771-1703-1 100 tablet, film coated in 1 bottle (70771-1703-1)
70771-1703-3 30 tablet, film coated in 1 bottle (70771-1703-3)
70771-1703-4 10 blister pack in 1 carton (70771-1703-4) / 10 tablet, film coated in 1 blister pack (70771-1703-2)
70771-1703-5 500 tablet, film coated in 1 bottle (70771-1703-5)
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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