NDC 13107-212
Hydrocodone Bitartrate and Acetaminophen 300 mg / 7.5 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, 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
- 300 mg / 7.5 mg
- Approval
- ANDA ANDA207709
- On the market since
- May 6, 2015
- Package NDCs
13107-212-0113107-212-0513107-212-3013107-212-99- Official label
- DailyMed (National Library of Medicine), updated Dec 17, 2025
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