Methocarbamol 70436-0149
Product NDC
70436-0149- Manufacturer
- Slate Run Pharmaceuticals, Llc
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- July 1, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA208116
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Methocarbamol | 100 mg/mL |
Drug Class
Muscle Relaxant [EPC]Centrally-mediated Muscle Relaxation [PE]Muscle Relaxant [EPC]
Packaging Options(1)
25 VIAL, SINGLE-DOSE in 1 CARTON (70436-149-55) / 10 mL in 1 VIAL, SINGLE-DOSE (70436-149-33)