Cyclobenzaprine Hydrochloride 80425-0019
Product NDC
80425-0019- Manufacturer
- Advanced Rx Of Tennessee, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 30, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA077797
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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)
30 TABLET, FILM COATED in 1 BOTTLE (80425-0019-1)
60 TABLET, FILM COATED in 1 BOTTLE (80425-0019-2)
90 TABLET, FILM COATED in 1 BOTTLE (80425-0019-3)