NDC 68071-2494
Hydrocodone Bitartrate and Acetaminophen 325 mg / 7.5 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Eywa Pharma Inc's NDC 71930-020.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Wes Pharma Inc | Westminster, MD, United States | Makes it, packages it and labels it | Problems found, fixed voluntarilyNov 20, 2025 · 7 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- tablet, oral
- Strength
- 325 mg / 7.5 mg
- Approval
- ANDA ANDA210211
- On the market since
- Jul 13, 2018
- Package NDCs
68071-2494-268071-2494-6- Official label
- DailyMed (National Library of Medicine), updated Mar 27, 2024
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