NDC 50090-1045 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-1045

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
A-S Medication Solutions
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075805
Marketed since
April 16, 2001
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
50090-1045-030 TABLET in 1 BOTTLE (50090-1045-0)Nov 28, 2014
50090-1045-120 TABLET in 1 BOTTLE (50090-1045-1)Nov 28, 2014
50090-1045-260 TABLET in 1 BOTTLE (50090-1045-2)Nov 28, 2014
50090-1045-390 TABLET in 1 BOTTLE (50090-1045-3)Mar 12, 2018

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