NDC Code | 21695-723-28 |
Package Description | 28 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (21695-723-28) |
Product NDC | 21695-723 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Amrix |
Non-Proprietary Name | Cyclobenzaprine Hydrochloride |
Dosage Form | CAPSULE, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20071001 |
Marketing Category Name | NDA |
Application Number | NDA021777 |
Manufacturer | Rebel Distributors Corp. |
Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
Strength | 15 |
Strength Unit | mg/1 |
Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |