NDC 70518-1585-6
Ondansetron Hydrochloride 4 mg/1
Ondansetron Hydrochloride · TABLET, FILM COATED
Ondansetron Hydrochloride is a tablet, film coated containing ondansetron hydrochloride at a strength of 4 mg/1. Manufactured by REMEDYREPACK INC..
Key Facts
- Brand Name
- Ondansetron Hydrochloride
- Generic Name
- Ondansetron Hydrochloride
- NDC Code (Package)
70518-1585-6- NDC Code (Product)
70518-1585- Manufacturer
- REMEDYREPACK INC.
- Strength
- 4 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA078539
- Marketing Start
- 10/24/2018
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.