NDC 71610-470 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-470

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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 (3)

Package NDCDescriptionSince
71610-470-5360 TABLET in 1 BOTTLE, PLASTIC (71610-470-53)Apr 7, 2021
71610-470-6090 TABLET in 1 BOTTLE, PLASTIC (71610-470-60)Oct 9, 2020
71610-470-80180 TABLET in 1 BOTTLE, PLASTIC (71610-470-80)Oct 9, 2020

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