NDC 87063-051
Hydrocodone Bitartrate and Acetaminophen 10 mg / 325 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Eywa Pharma Inc's NDC 71930-021.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Wes Pharma Inc | Westminster, MD, United States | Makes it, packages it and labels it | Problems found, fixed voluntarilyNov 20, 2025 · 7 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 ANDA210211
- On the market since
- Jul 13, 2018
- Package NDCs
87063-051-0187063-051-0587063-051-0787063-051-1087063-051-1487063-051-2087063-051-3087063-051-6087063-051-90- Official label
- DailyMed (National Library of Medicine), updated Mar 10, 2026
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