NDC 50090-7178 – Famotidine

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

Human Prescription Drug

Product NDC50090-7178

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215767
Marketed since
November 4, 2021
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
50090-7178-030 TABLET, FILM COATED in 1 BOTTLE (50090-7178-0)May 30, 2024
50090-7178-120 TABLET, FILM COATED in 1 BOTTLE (50090-7178-1)May 30, 2024
50090-7178-260 TABLET, FILM COATED in 1 BOTTLE (50090-7178-2)May 30, 2024
50090-7178-390 TABLET, FILM COATED in 1 BOTTLE (50090-7178-3)May 30, 2024

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