NDC 66336-722
Oxaprozin 600 mg tablet
On the label: Dispensing Solutions Inc.. It's repackaged from NDC 0185-0141, made by Eon Labs, Inc. (Oxaprozin). 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 (it lists 1 site that repackages it and relabels it). 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 Dispensing Solutions Inc. names for other drugs.
Product details
- Generic drug
- Oxaprozin: every company that makes it
- Form
- tablet
- Strength
- 600 mg
- Approval
- ANDA ANDA075845
- On the market since
- Jan 31, 2001
- Package NDCs
66336-722-60- Official label
- DailyMed (National Library of Medicine), updated Jul 3, 2013
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