NDC 51655-312 – Famotidine

Famotidine 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-312

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075805
Marketed since
May 21, 2020
Listing expires
December 31, 2027
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (2)

Package NDCDescriptionSince
51655-312-2020 TABLET in 1 BOTTLE, PLASTIC (51655-312-20)May 22, 2020
51655-312-2560 TABLET in 1 BOTTLE, PLASTIC (51655-312-25)May 21, 2020

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