NDC 17856-0920
Oxycodone Hydrochloride 20 mg per 1 mL solution
On the label: Atlantic Biologicals Corps.. It's repackaged: Atlantic Biologicals Corps. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 43386-920.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Novel Laboratories, Inc. | Somerset, NJ, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action |
Repackaging site
- Atlantic Biologicals Corps, Location not on file · repackages it and relabels it
Product details
- Generic drug
- Oxycodone: every company that makes it
- Form
- solution
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA204603
- On the market since
- May 22, 2018
- Package NDCs
17856-0920-117856-0920-217856-0920-317856-0920-417856-0920-517856-0920-617856-0920-717856-0920-8- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2021
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