NDC 71205-257 – Famotidine

Famotidine 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-257

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Proficient Rx LP
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
71205-257-3030 TABLET in 1 BOTTLE (71205-257-30)Jul 23, 2020
71205-257-6060 TABLET in 1 BOTTLE (71205-257-60)Jul 23, 2020
71205-257-9090 TABLET in 1 BOTTLE (71205-257-90)Jul 23, 2020

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