NDC 13107-019
Hydrocodone Bitartrate and Acetaminophen 5 mg / 325 mg tablet
On the label: Aurolife Pharma LLC.
Where it's 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 |
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
13107-019-0113107-019-0513107-019-3013107-019-99- Official label
- DailyMed (National Library of Medicine), updated Dec 11, 2025
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