Methocarbamol 85509-1341
Product NDC
85509-1341- Manufacturer
- Phoenix Rx Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 12, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA213967
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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(2)
30 TABLET, FILM COATED in 1 BOTTLE (85509-1341-3)
60 TABLET, FILM COATED in 1 BOTTLE (85509-1341-6)