NDC 68382-444 – Famotidine

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

Human Prescription Drug

Product NDC68382-444

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA091020
Marketed since
April 22, 2021
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
68382-444-0550 mL in 1 BOTTLE, PLASTIC (68382-444-05)Apr 22, 2021

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