NDC 72789-499
Methocarbamol Tablets, USP, 500 mg 500 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 63561-0173.
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
- 500 mg
- Approval
- ANDA ANDA212623
- On the market since
- Jan 1, 2024
- Package NDCs
72789-499-1872789-499-2072789-499-28- Official label
- DailyMed (National Library of Medicine), updated Nov 4, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?