NDC 68071-4853
Hydrocodone Bitartrate and Acetaminophen 5 mg / 325 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Aurolife Pharma LLC's NDC 13107-019.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it, tests it, packages it and labels it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
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
- 5 mg / 325 mg
- Approval
- ANDA ANDA201013
- On the market since
- Apr 11, 2012
- Package NDCs
68071-4853-2- Official label
- DailyMed (National Library of Medicine), updated Jun 14, 2024
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