NDC 17856-0826
Oxycodone Hydrochloride 100 mg per 5 mL solution
On the label: Atlantic Biologicals Corps.. It's repackaged from NDC 0121-0826, made by PAI Holdings, LLC dba PAI Pharma (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 (it lists 1 site that repackages it). 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 Atlantic Biologicals Corps. names for other drugs.
Product details
- Generic drug
- Oxycodone: every company that makes it
- Form
- solution
- Strength
- 100 mg per 5 mL
- Approval
- ANDA ANDA206822
- On the market since
- Jun 4, 2018
- Package NDCs
17856-0826-117856-0826-217856-0826-317856-0826-417856-0826-517856-0826-6- Official label
- DailyMed (National Library of Medicine), updated May 15, 2024
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