NDC 85509-1341
Methocarbamol 750 mg tablet, film coated
On the label: Phoenix RX LLC. It's repackaged: Phoenix RX LLC rebottles it from Aurobindo Pharma Limited's NDC 59651-341.
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
- Phoenix RX LLC, Hatboro, PA, United States · repackages it and relabels it
Product details
- Generic drug
- Methocarbamol: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 750 mg
- Approval
- ANDA ANDA213967
- On the market since
- Aug 12, 2020
- Package NDCs
85509-1341-385509-1341-6- Official label
- DailyMed (National Library of Medicine), updated Jul 29, 2025
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