NDC 67296-1655
Hydrocodone Bitartrate and Ibuprofen 200 mg / 7.5 mg tablet, film coated
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Aurolife Pharma LLC's NDC 13107-004.
Where the pills inside were 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 |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Hydrocodone and Ibuprofen: every company that makes it
- Form
- tablet, film coated
- Strength
- 200 mg / 7.5 mg
- Approval
- ANDA ANDA204575
- On the market since
- Jan 1, 2019
- Package NDCs
67296-1655-7- Official label
- DailyMed (National Library of Medicine), updated Aug 9, 2024
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