NDC 64980-737 – Famotidine

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

Human Prescription Drug

Product NDC64980-737

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
RISING PHARMA HOLDINGS, INC.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA217655
Marketed since
August 20, 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
64980-737-5050 mL in 1 BOTTLE (64980-737-50)Aug 20, 2026

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