NDC 31722-063 – Famotidine

Famotidine 40 mg/5mL · Powder, For Suspension · Oral

Human Prescription Drug

Product NDC31722-063

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA217330
Marketed since
August 17, 2023
Listing expires
December 31, 2026
Pharmacologic class
Histamine-2 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Famotidine →

Package NDC codes (1)

Package NDCDescriptionSince
31722-063-3150 mL in 1 BOTTLE (31722-063-31)Aug 17, 2023

Other Famotidine products