Famotidine

Product NDC
71335-2805
11-digit product format
713352805
Labeler code
71335
Product ID
71335-2805_b2d70cef-4104-46d3-af20-aec60436b34b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA217400
Marketing category
ANDA
Marketing start
2024-08-06
Substance
FAMOTIDINE
Active strength
20 mg/1
Pharmacologic classes
Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
5QZO15J2Z8FAMOTIDINE76824-35-6FAMOTIDINE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71335-2805-07133528050040 TABLET, FILM COATED in 1 BOTTLE (71335-2805-0) 2025-10-14NoNoHistorical
71335-2805-17133528050130 TABLET, FILM COATED in 1 BOTTLE (71335-2805-1) 2025-10-14NoNoHistorical
71335-2805-27133528050260 TABLET, FILM COATED in 1 BOTTLE (71335-2805-2) 2025-10-14NoNoHistorical
71335-2805-37133528050320 TABLET, FILM COATED in 1 BOTTLE (71335-2805-3) 2025-10-14NoNoHistorical
71335-2805-47133528050490 TABLET, FILM COATED in 1 BOTTLE (71335-2805-4) 2025-10-14NoNoHistorical
71335-2805-571335280505100 TABLET, FILM COATED in 1 BOTTLE (71335-2805-5) 2025-10-14NoNoHistorical
71335-2805-67133528050610 TABLET, FILM COATED in 1 BOTTLE (71335-2805-6) 2025-10-14NoNoHistorical
71335-2805-771335280507120 TABLET, FILM COATED in 1 BOTTLE (71335-2805-7) 2025-10-14NoNoHistorical
71335-2805-87133528050850 TABLET, FILM COATED in 1 BOTTLE (71335-2805-8) 2025-10-14NoNoHistorical
71335-2805-97133528050914 TABLET, FILM COATED in 1 BOTTLE (71335-2805-9) 2025-10-14NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
FamotidineBryant Ranch Prepack2025-10-14HUMAN PRESCRIPTION DRUG LABEL1