NDC 13107-004
Hydrocodone Bitartrate and Ibuprofen 200 mg / 7.5 mg tablet, film coated
On the label: Aurolife Pharma LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
Product details
- Generic drug
- Hydrocodone and Ibuprofen: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 200 mg / 7.5 mg
- Approval
- ANDA ANDA204575
- On the market since
- Jun 2, 2016
- Package NDCs
13107-004-0113107-004-0513107-004-1113107-004-99- Official label
- DailyMed (National Library of Medicine), updated Dec 23, 2025
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