NDC 67296-1623
Hydrocodone Bitartrate and Acetaminophen 5 mg / 325 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from KVK-TECH, Inc.'s NDC 10702-189.
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
- 5 mg / 325 mg
- Approval
- ANDA ANDA209037
- On the market since
- Jan 1, 2018
- Package NDCs
67296-1623-067296-1623-167296-1623-267296-1623-367296-1623-467296-1623-567296-1623-667296-1623-767296-1623-867296-1623-9- Official label
- DailyMed (National Library of Medicine), updated Jul 24, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?