NDC 17856-0023
Oxycodone Hydrochloride 20 mg per 1 mL solution
On the label: Atlantic Biologicals Corps.. It's repackaged: Atlantic Biologicals Corps. rebottles it from Eywa Pharma Inc's NDC 71930-023.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Wes Pharma Inc | Westminster, MD, United States | Makes it, packages it and labels it | Problems found, fixed voluntarilyNov 20, 2025 · 7 inspections |
Repackaging site
- Atlantic Biologicals Corps, Location not on file · repackages it
Product details
- Generic drug
- Oxycodone: every company that makes it
- Form
- solution
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA209897
- On the market since
- Jun 1, 2018
- Package NDCs
17856-0023-117856-0023-217856-0023-317856-0023-417856-0023-517856-0023-6- Official label
- DailyMed (National Library of Medicine), updated May 9, 2023
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