Acid Controller

Product NDC
59640-001
Type
HUMAN OTC DRUG
Nonproprietary name
famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
H E B
Application
ANDA077351
Marketing category
ANDA
Substance
FAMOTIDINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
59640-001-631 BOTTLE in 1 CARTON (59640-001-63) / 25 TABLET, FILM COATED in 1 BOTTLE2022-06-06NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
HEB Acid Controller Drug FactsH E B2025-10-30HUMAN OTC DRUG LABEL3
HEB Acid Controller Drug FactsH E B2022-06-14HUMAN OTC DRUG LABEL2