NDC 57896-319 – Famotidine

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

Human Otc Drug

Product NDC57896-319

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Geri-Care Pharmaceutical Corp
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215822
Marketed since
April 1, 2024
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
57896-319-011 BOTTLE in 1 CARTON (57896-319-01) / 100 TABLET, FILM COATED in 1 BOTTLEApr 1, 2024

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