NDC 72789-521
Methocarbamol Tablets, USP, 750 mg 750 mg tablet, film coated
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Granulation Technology, Inc.'s NDC 63561-0174.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Granulation Technology, Inc. | Fairfield, NJ, United States | Makes it | Not inspected on record |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Methocarbamol: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 750 mg
- Approval
- ANDA ANDA212623
- On the market since
- Jun 10, 2025
- Package NDCs
72789-521-2072789-521-3072789-521-4072789-521-6072789-521-82- Official label
- DailyMed (National Library of Medicine), updated Mar 23, 2026
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