NDC 72789-034 – Ondansetron Hydrochloride

Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72789-034

Product details

Brand name
Ondansetron Hydrochloride
Generic name
Ondansetron Hydrochloride
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078539
Marketed since
July 31, 2007
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
72789-034-1212 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-034-12)Dec 2, 2019

Other Ondansetron hydrochloride products