NDC 87063-040
Methocarbamol 500 mg tablet, film coated
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-340.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Methocarbamol: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA213967
- On the market since
- Feb 9, 2023
- Package NDCs
87063-040-0187063-040-1087063-040-2087063-040-3087063-040-6087063-040-90- Official label
- DailyMed (National Library of Medicine), updated Nov 24, 2025
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