NDC 0143-9771
Ondansetron Hydrochloride and Dextrose 32 mg per 50 mL injection, solution
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Hikma Pharmaceuticals USA Inc. names for other drugs.
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- injection, solution
- Strength
- 32 mg per 50 mL
- Approval
- ANDA ANDA078308
- On the market since
- Aug 4, 2009
- Package NDCs
0143-9771-06- Official label
- DailyMed (National Library of Medicine), updated Feb 2, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?