FAMOTIDINE

Product NDC
71335-9748
11-digit product format
713359748
Labeler code
71335
Product ID
71335-9748_c1158423-fee4-475a-a9ec-fd6dc16c5a8f
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
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
71335-9748-17133597480130 TABLET, FILM COATED in 1 BOTTLE (71335-9748-1) 2023-09-14NoNoHistorical
71335-9748-27133597480260 TABLET, FILM COATED in 1 BOTTLE (71335-9748-2) 2023-10-03NoNoHistorical
71335-9748-37133597480320 TABLET, FILM COATED in 1 BOTTLE (71335-9748-3) 2023-09-18NoNoHistorical
71335-9748-47133597480490 TABLET, FILM COATED in 1 BOTTLE (71335-9748-4) 2023-09-05NoNoHistorical
71335-9748-571335974805100 TABLET, FILM COATED in 1 BOTTLE (71335-9748-5) 2023-11-17NoNoHistorical
71335-9748-67133597480610 TABLET, FILM COATED in 1 BOTTLE (71335-9748-6) 2024-04-05NoNoHistorical
71335-9748-771335974807120 TABLET, FILM COATED in 1 BOTTLE (71335-9748-7) 2024-03-26NoNoHistorical
71335-9748-87133597480850 TABLET, FILM COATED in 1 BOTTLE (71335-9748-8) 2024-04-05NoNoHistorical
71335-9748-97133597480914 TABLET, FILM COATED in 1 BOTTLE (71335-9748-9) 2024-04-05NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
FAMOTIDINEBryant Ranch Prepack2025-03-31HUMAN PRESCRIPTION DRUG LABEL103