Drugplain

NDC 51655-016-53

Ondansetron Hydrochloride 8 mg/1

Ondansetron Hydrochloride · TABLET, FILM COATED

No Recall History

Ondansetron Hydrochloride is a tablet, film coated containing ondansetron hydrochloride at a strength of 8 mg/1. Manufactured by Northwind Health Company, LLC.

Key Facts

Brand Name
Ondansetron Hydrochloride
Generic Name
Ondansetron Hydrochloride
NDC Code (Package)
51655-016-53
NDC Code (Product)
51655-016
Manufacturer
Northwind Health Company, LLC
Strength
8 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA078539
Marketing Start
08/08/2022

Recall History

No Recall History

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