Methocarbamol 72789-0110
Product NDC
72789-0110- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 15, 2018
- Listing Expires
- December 31, 2027
- Application
- ANDA208507
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Methocarbamol | 500 mg/1 |
Drug Class
Muscle Relaxant [EPC]Centrally-mediated Muscle Relaxation [PE]Muscle Relaxant [EPC]
Packaging Options(1)
40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-110-40)