NDC 76420-713 – Famotidine

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

Human Prescription Drug

Product NDC76420-713

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215630
Marketed since
August 23, 2023
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (4)

Package NDCDescriptionSince
76420-713-01100 TABLET, FILM COATED in 1 BOTTLE (76420-713-01)Apr 11, 2024
76420-713-3030 TABLET, FILM COATED in 1 BOTTLE (76420-713-30)Apr 11, 2024
76420-713-6060 TABLET, FILM COATED in 1 BOTTLE (76420-713-60)Apr 11, 2024
76420-713-9090 TABLET, FILM COATED in 1 BOTTLE (76420-713-90)Apr 11, 2024

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