NDC 58602-828 – Famotidine

Famotidine 10 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC58602-828

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Aurohealth LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206531
Marketed since
April 26, 2016
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
58602-828-191 BOTTLE in 1 CARTON (58602-828-19) / 90 TABLET, FILM COATED in 1 BOTTLEApr 26, 2016

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