NDC 76420-768
Oxycodone hydrochloride 30 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Alvogen Inc.'s NDC 47781-265.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Norwich Pharmaceuticals, Inc. | Norwich, NY, United States | Makes it, tests it and packages it | No problems foundMay 1, 2026 · 8 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Oxycodone: every company that makes it
- Form
- tablet, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA202116
- On the market since
- Dec 30, 2011
- Package NDCs
76420-768-0176420-768-0576420-768-1076420-768-2076420-768-3076420-768-6076420-768-90- Official label
- DailyMed (National Library of Medicine), updated Jun 25, 2024
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