NDC 70518-4574 – Famotidine

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

Human Prescription Drug

Product NDC70518-4574

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215630
Marketed since
February 16, 2026
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (4)

Package NDCDescriptionSince
70518-4574-010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4574-0)Feb 16, 2026
70518-4574-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4574-1)Mar 4, 2026
70518-4574-280 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4574-2)Mar 10, 2026
70518-4574-360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4574-3)Apr 2, 2026

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