Cyclobenzaprine Hydrochloride 68071-3462
Product NDC
68071-3462- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 31, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA208170
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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(3)
20 TABLET, FILM COATED in 1 BOTTLE (68071-3462-2)
30 TABLET, FILM COATED in 1 BOTTLE (68071-3462-3)
15 TABLET, FILM COATED in 1 BOTTLE (68071-3462-5)