Methocarbamol 70868-0901
Product NDC
70868-0901- Manufacturer
- Key Therapeutics
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 26, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA040489
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Methocarbamol | 750 mg/1 |
Drug Class
Muscle Relaxant [EPC]Centrally-mediated Muscle Relaxation [PE]Muscle Relaxant [EPC]
Packaging Options(1)
90 TABLET in 1 BOTTLE (70868-901-90)