Cyclobenzaprine Hydrochloride 68071-2659
Product NDC
68071-2659- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 26, 2008
- Listing Expires
- December 31, 2026
- Application
- ANDA078643
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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(4)
30 TABLET, FILM COATED in 1 BOTTLE (68071-2659-3)
15 TABLET, FILM COATED in 1 BOTTLE (68071-2659-5)
6 TABLET, FILM COATED in 1 BOTTLE (68071-2659-6)
14 TABLET, FILM COATED in 1 BOTTLE (68071-2659-7)