NDC 87441-030 – Famotidine

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

Human Prescription Drug

Product NDC87441-030

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Unit Dose Solutions, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206530
Marketed since
June 22, 2026
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (1)

Package NDCDescriptionSince
87441-030-0130 TABLET, FILM COATED in 1 BLISTER PACK (87441-030-01)Jun 22, 2026

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