NDC 71610-399 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-399

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078916
Marketed since
January 29, 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 (3)

Package NDCDescriptionSince
71610-399-3030 TABLET in 1 BOTTLE (71610-399-30)Jun 23, 2020
71610-399-6090 TABLET in 1 BOTTLE (71610-399-60)Feb 21, 2020
71610-399-80180 TABLET in 1 BOTTLE (71610-399-80)Feb 21, 2020

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