Cyclobenzaprine Hydrochloride 51655-0539
Product NDC
51655-0539- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 14, 2021
- Listing Expires
- December 31, 2027
- 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, PLASTIC (51655-539-20)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-52)
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-53)