NDC 72789-345 – Famotidine

Famotidine 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72789-345

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215630
Marketed since
July 8, 2022
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (1)

Package NDCDescriptionSince
72789-345-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-345-30)Aug 7, 2023

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