NDC 50090-6582 – Famotidine

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

Human Prescription Drug

Product NDC50090-6582

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215630
Marketed since
July 8, 2022
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
50090-6582-030 TABLET, FILM COATED in 1 BOTTLE (50090-6582-0)Aug 9, 2023
50090-6582-120 TABLET, FILM COATED in 1 BOTTLE (50090-6582-1)Aug 9, 2023
50090-6582-260 TABLET, FILM COATED in 1 BOTTLE (50090-6582-2)Aug 9, 2023
50090-6582-390 TABLET, FILM COATED in 1 BOTTLE (50090-6582-3)Aug 9, 2023

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