NDC 67296-1618
Hydrocodone Bitartrate and Acetaminophen 325 mg / 7.5 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from KVK-TECH, Inc.'s NDC 10702-190.
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
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- tablet
- Strength
- 325 mg / 7.5 mg
- Approval
- ANDA ANDA209037
- On the market since
- Jan 1, 2018
- Package NDCs
67296-1618-167296-1618-367296-1618-667296-1618-9- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2022
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