NDC 0338-5197 – Famotidine

Famotidine 20 mg/50mL · Injection, Solution · Intravenous

Human Prescription Drug 2 recalls

Product NDC0338-5197

Product details

Brand name
Famotidine
Generic name
Famotidine
Labeler
Baxter Healthcare Corporation
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA075591
Marketed since
May 10, 2001
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
0338-5197-4112 BAG in 1 CARTON (0338-5197-41) / 50 mL in 1 BAGMay 10, 2001

Recalls mentioning this NDC

Other Famotidine products