Cyclobenzaprine Hydrochloride 42708-0172
Product NDC
42708-0172- Manufacturer
- Qpharma 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 | 5 mg/1 |
Drug Class
Centrally-mediated Muscle Relaxation [PE]Muscle Relaxant [EPC]
Packaging Options(1)
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-172-20)