NDC 52959-245
Ketoprofen 50 mg capsule
On the label: H.J. Harkins Co., Inc.. It's repackaged from NDC 0093-3193, made by Teva Pharmaceuticals USA, Inc. (Ketoprofen). 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
- Ketoprofen: every company that makes it
- Form
- capsule
- Strength
- 50 mg
- Approval
- ANDA ANDA073516
- On the market since
- Jan 18, 2011
- Package NDCs
52959-245-1452959-245-1552959-245-2052959-245-2152959-245-3052959-245-6052959-245-90- Official label
- DailyMed (National Library of Medicine), updated Aug 29, 2011
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