NDC 71335-0231 – Famotidine

Famotidine 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0231

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078916
Marketed since
January 29, 2016
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (8)

Package NDCDescriptionSince
71335-0231-130 TABLET in 1 BOTTLE (71335-0231-1)Jul 26, 2018
71335-0231-260 TABLET in 1 BOTTLE (71335-0231-2)Mar 6, 2018
71335-0231-3100 TABLET in 1 BOTTLE (71335-0231-3)Nov 11, 2019
71335-0231-490 TABLET in 1 BOTTLE (71335-0231-4)Jul 16, 2018
71335-0231-515 TABLET in 1 BOTTLE (71335-0231-5)Jan 31, 2019
71335-0231-6120 TABLET in 1 BOTTLE (71335-0231-6)Dec 27, 2021
71335-0231-720 TABLET in 1 BOTTLE (71335-0231-7)Dec 27, 2021
71335-0231-810 TABLET in 1 BOTTLE (71335-0231-8)Dec 27, 2021

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