NDC 70518-4395 – Famotidine

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

Human Prescription Drug

Product NDC70518-4395

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA217400
Marketed since
July 21, 2025
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (2)

Package NDCDescriptionSince
70518-4395-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4395-0)Jul 21, 2025
70518-4395-150 POUCH in 1 BOX (70518-4395-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-4395-2)Apr 23, 2026

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