NDC 67296-1791
Hydrocodone Bitartrate and Acetaminophen 5 mg / 325 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Aurolife Pharma LLC's NDC 13107-019.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it, tests it, packages it and labels 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
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- tablet
- Strength
- 5 mg / 325 mg
- Approval
- ANDA ANDA201013
- On the market since
- Apr 11, 2012
- Package NDCs
67296-1791-167296-1791-267296-1791-367296-1791-567296-1791-667296-1791-767296-1791-867296-1791-9- Official label
- DailyMed (National Library of Medicine), updated Jul 25, 2024
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