NDC 43386-500 – Famotidine

Famotidine 40 mg/5mL · For Suspension · Oral

Human Prescription Drug 1 recall

Product NDC43386-500

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Lupin Pharmaceuticals,Inc.
Dosage form
For Suspension
Route
Oral
Marketing category
ANDA · ANDA201695
Marketed since
December 17, 2012
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
43386-500-1150 mL in 1 BOTTLE (43386-500-11)Dec 17, 2012

Recalls mentioning this NDC

Other Famotidine products