NDC 31722-017 – Famotidine

Famotidine 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC31722-017

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215767
Marketed since
November 4, 2021
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (2)

Package NDCDescriptionSince
31722-017-01100 TABLET, FILM COATED in 1 BOTTLE (31722-017-01)Nov 4, 2021
31722-017-101000 TABLET, FILM COATED in 1 BOTTLE (31722-017-10)Nov 4, 2021

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