Famotidine

Product NDC
69842-928
Type
HUMAN OTC DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
CVS Pharmacy, Inc.
Application
ANDA206531
Marketing category
ANDA
Substance
FAMOTIDINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
69842-928-841 BOTTLE in 1 CARTON (69842-928-84) / 30 TABLET, FILM COATED in 1 BOTTLE2021-06-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Famotidine - CVS Pharmacy, Inc. | Aurohealth LLC | Aurobindo Pharma Limited | APL HEALTHCARE LIMITEDCVS Pharmacy, Inc. | Aurohealth LLC | Aurobindo Pharma Limited | APL HEALTHCARE LIMITED2025-03-28Human OTC Drug Label4