FAMOTIDINE

Product NDC
71335-9724
11-digit product format
713359724
Labeler code
71335
Product ID
71335-9724_e5c1db20-4893-4dc8-b577-a649ab230c8c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
FAMOTIDINE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA215630
Marketing category
ANDA
Marketing start
2022-07-08
Substance
FAMOTIDINE
Active strength
40 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
71335-9724-17133597240130 TABLET, FILM COATED in 1 BOTTLE (71335-9724-1) 2023-05-30NoNoHistorical
71335-9724-27133597240260 TABLET, FILM COATED in 1 BOTTLE (71335-9724-2) 2023-05-30NoNoHistorical
71335-9724-371335972403100 TABLET, FILM COATED in 1 BOTTLE (71335-9724-3) 2023-05-30NoNoHistorical
71335-9724-47133597240490 TABLET, FILM COATED in 1 BOTTLE (71335-9724-4) 2023-05-30NoNoHistorical
71335-9724-57133597240515 TABLET, FILM COATED in 1 BOTTLE (71335-9724-5) 2023-05-30NoNoHistorical
71335-9724-671335972406120 TABLET, FILM COATED in 1 BOTTLE (71335-9724-6) 2023-05-30NoNoHistorical
71335-9724-77133597240720 TABLET, FILM COATED in 1 BOTTLE (71335-9724-7) 2023-05-30NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
FAMOTIDINEBryant Ranch Prepack2024-08-23HUMAN PRESCRIPTION DRUG LABEL102