NDC 36000-012 – Ondansetron Hydrochloride

Ondansetron Hydrochloride 2 mg/mL · Solution · Intramuscular, Intravenous

Human Prescription Drug 1 recall

Product NDC36000-012

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
Baxter Healthcare Corporation
Dosage form
Solution
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA078287
Marketed since
March 13, 2013
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
36000-012-2525 VIAL, SINGLE-DOSE in 1 CARTON (36000-012-25) / 2 mL in 1 VIAL, SINGLE-DOSEMar 13, 2013

Recalls mentioning this NDC

Other Ondansetron hydrochloride products