NDC 54868-5902
Oxycodone Hydrochloride 20 mg tablet
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 58177-462, made by Ethex Corporation (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 Physicians Total Care, Inc. names for other drugs.
Product details
- Generic drug
- Oxycodone: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA077290
- On the market since
- Jun 6, 2008
- Package NDCs
54868-5902-054868-5902-154868-5902-254868-5902-3- Official label
- DailyMed (National Library of Medicine), updated Jan 11, 2010
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