NDC 67296-1334
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 Rhodes Pharmaceuticals L.P.'s NDC 42858-202.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Knoa Pharmaceuticals LLC | Wilson, NC, United States | Makes it | Problems found, fixed voluntarilySep 26, 2025 · 9 inspections |
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 ANDA202991
- On the market since
- Apr 12, 2016
- Package NDCs
67296-1334-3- Official label
- DailyMed (National Library of Medicine), updated Jan 20, 2022
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