NDC 68180-150 – Famotidine

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

Human Prescription Drug 1 recall

Product NDC68180-150

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Powder, For Suspension
Route
Oral
Marketing category
ANDA · ANDA090440
Marketed since
June 29, 2010
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
68180-150-0150 mL in 1 BOTTLE (68180-150-01)Jun 29, 2010

Recalls mentioning this NDC

Other Famotidine products