Cyclobenzaprine Hydrochloride 16571-0783
Product NDC
16571-0783- Manufacturer
- Rising Pharma Holdings, 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(3)
100 TABLET, FILM COATED in 1 BOTTLE (16571-783-01)
1000 TABLET, FILM COATED in 1 BOTTLE (16571-783-10)
500 TABLET, FILM COATED in 1 BOTTLE (16571-783-50)