NDC 72887-648
oxycodone hydrochloride and acetaminophen 10 mg per 5 mL / 300 mg per 5 mL solution
On the label: FH2 Pharma LLC.
Where it's 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 FH2 Pharma LLC names for other drugs.
Product details
- Generic drug
- Acetaminophen and Oxycodone: every company that makes it
- Form
- solution, oral
- Strength
- 10 mg per 5 mL / 300 mg per 5 mL
- Approval
- ANDA ANDA202142
- On the market since
- Mar 1, 2020
- Package NDCs
72887-648-12- Official label
- DailyMed (National Library of Medicine), updated Apr 27, 2026
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