Methocarbamol 72887-0873
Product NDC
72887-0873- Manufacturer
- Fh2 Pharma Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 30, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA212707
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Methocarbamol | 1000 mg/1 |
Drug Class
Muscle Relaxant [EPC]Centrally-mediated Muscle Relaxation [PE]Muscle Relaxant [EPC]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72887-873-03)