NDC 54348-821-00
Ondansetron Hydrochloride 8 mg/1
Ondansetron Hydrochloride · TABLET, FILM COATED
Ondansetron Hydrochloride is a tablet, film coated containing ondansetron hydrochloride at a strength of 8 mg/1. Manufactured by Pharmpak, Inc..
Key Facts
- Brand Name
- Ondansetron Hydrochloride
- Generic Name
- Ondansetron Hydrochloride
- NDC Code (Package)
54348-821-00- NDC Code (Product)
54348-821- Manufacturer
- Pharmpak, Inc.
- Strength
- 8 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA078539
- Marketing Start
- 08/08/2019
Recall History
No Recall HistoryView Full Drug Page
Ondansetron Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.