NDC 68001-397 – Famotidine

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

Human Prescription Drug

Product NDC68001-397

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
BluePoint Laboratories
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206530
Marketed since
June 19, 2019
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (2)

Package NDCDescriptionSince
68001-397-00100 TABLET, FILM COATED in 1 BOTTLE (68001-397-00)Jun 19, 2019
68001-397-081000 TABLET, FILM COATED in 1 BOTTLE (68001-397-08)Jun 19, 2019

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