Methocarbamol 68788-8880
Product NDC
68788-8880- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 2, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA203550
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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(3)
30 TABLET, FILM COATED in 1 BOTTLE (68788-8880-3)
60 TABLET, FILM COATED in 1 BOTTLE (68788-8880-6)
90 TABLET, FILM COATED in 1 BOTTLE (68788-8880-9)