NDC 52959-129
Oxycodone Hydrochloride 15 mg tablet
On the label: H.J. Harkins Co., Inc.. It's repackaged from NDC 0603-4991, made by Par Pharmaceutical (Oxycodone Hydrochloride). 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
- Oxycodone: every company that makes it
- Form
- tablet
- Strength
- 15 mg
- Approval
- ANDA ANDA077712
- On the market since
- Jan 31, 2007
- Package NDCs
52959-129-0252959-129-3052959-129-6052959-129-90- Official label
- DailyMed (National Library of Medicine), updated Dec 15, 2011
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