NDC 76420-215
Hydrocodone Bitartrate and Acetaminophen 10 mg / 325 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Rhodes Pharmaceuticals L.P.'s NDC 42858-203.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Knoa Pharmaceuticals LLC | Wilson, NC, United States | Makes it | Problems found, fixed voluntarilySep 26, 2025 · 9 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg / 325 mg
- Approval
- ANDA ANDA202991
- On the market since
- Apr 12, 2016
- Package NDCs
76420-215-0176420-215-3076420-215-6076420-215-90- Official label
- DailyMed (National Library of Medicine), updated May 10, 2022
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