NDC 51655-804
Hydrocodone Bitartrate and Acetaminophen 325 mg / 7.5 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Aurolife Pharma LLC's NDC 13107-020.
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
- EPM Packaging, Location not on file · repackages it
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- tablet
- Strength
- 325 mg / 7.5 mg
- Approval
- ANDA ANDA201013
- On the market since
- Jul 31, 2015
- Package NDCs
51655-804-27- Official label
- DailyMed (National Library of Medicine), updated Jul 31, 2015
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