NDC 87063-049
Hydrocodone Bitartrate and Acetaminophen 5 mg / 325 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Eywa Pharma Inc's NDC 71930-019.
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
- 5 mg / 325 mg
- Approval
- ANDA ANDA210211
- On the market since
- Jul 13, 2018
- Package NDCs
87063-049-0187063-049-0587063-049-0787063-049-1087063-049-1487063-049-2087063-049-3087063-049-6087063-049-90- Official label
- DailyMed (National Library of Medicine), updated Mar 10, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?