Drug Information
Identification
Generic Name
Cyclobenzaprine Hydrochloride
Brand Name
Cyclobenzaprine Hydrochloride
Labeler / Distributor
Rising Pharma Holdings, Inc.
Product Type
HUMAN PRESCRIPTION DRUG
Administration
Dosage Form
TABLET, FILM COATED
Route of Administration
ORAL
FDA Application Number
ANDA078643
Active Ingredients
| Ingredient | Strength |
|---|---|
| CYCLOBENZAPRINE HYDROCHLORIDE | 5 mg/1 |
Pharmacological Class
Centrally-mediated Muscle Relaxation [PE]Muscle Relaxant
Data sourced from openFDA / DailyMed. For full prescribing information, consult the drug label.