NDC 52959-991
Ondansetron Hydrochloride 4 mg tablet, film coated
On the label: H.J. Harkins Co., Inc.. It's repackaged from NDC 0781-1679, made by Sandoz Inc (Ondansetron). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were 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 H.J. Harkins Co., Inc. names for other drugs.
Product details
- Generic drug
- Ondansetron: every company that makes it
- Form
- tablet, film coated
- Strength
- 4 mg
- Approval
- ANDA ANDA077517
- On the market since
- Jun 25, 2007
- Package NDCs
52959-991-03- Official label
- DailyMed (National Library of Medicine), updated Dec 20, 2011
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