Cyclobenzaprine Hydrochloride 70512-0872
Product NDC
70512-0872- Manufacturer
- Sola Pharmaceuticals, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 31, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA077563
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cyclobenzaprine Hydrochloride | 10 mg/1 |
Drug Class
Centrally-mediated Muscle Relaxation [PE]Muscle Relaxant [EPC]
Packaging Options(1)
100 TABLET, FILM COATED in 1 BOTTLE (70512-872-10)