NDC 67296-1631
Hydrocodone Bitartrate and Acetaminophen 10 mg / 325 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from KVK-TECH, Inc.'s NDC 10702-191.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Kvk-Tech, Inc. | Newtown, PA, United States | Makes it | Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it and relabels it
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- tablet
- Strength
- 10 mg / 325 mg
- Approval
- ANDA ANDA209037
- On the market since
- Jan 1, 2019
- Package NDCs
67296-1631-167296-1631-2- Official label
- DailyMed (National Library of Medicine), updated Jan 13, 2021
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