NDC 72789-331 – Famotidine

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

Human Prescription Drug

Product NDC72789-331

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
PD-Rx 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 (6)

Package NDCDescriptionSince
72789-331-022 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-02)Jul 30, 2024
72789-331-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-20)Jul 10, 2023
72789-331-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-30)Aug 1, 2023
72789-331-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-60)Jul 28, 2023
72789-331-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-90)Jul 17, 2023
72789-331-93180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-93)Aug 7, 2023

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