Drugplain

NDC 42708-044-05

Ondansetron Hydrochloride 4 mg/1

Ondansetron Hydrochloride · TABLET, FILM COATED

No Recall History

Ondansetron Hydrochloride is a tablet, film coated containing ondansetron hydrochloride at a strength of 4 mg/1. Manufactured by QPharma, Inc..

Key Facts

Brand Name
Ondansetron Hydrochloride
Generic Name
Ondansetron Hydrochloride
NDC Code (Package)
42708-044-05
NDC Code (Product)
42708-044
Manufacturer
QPharma, Inc.
Strength
4 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA078539
Marketing Start
07/31/2007

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.