NDC Code | 33261-033-21 |
Package Description | 21 TABLET in 1 BOTTLE, PLASTIC (33261-033-21) |
Product NDC | 33261-033 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Cyclobenzaprine Hydrochloride |
Non-Proprietary Name | Cyclobenzaprine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20100218 |
Marketing Category Name | ANDA |
Application Number | ANDA078218 |
Manufacturer | Aidarex Pharmaceuticals LLC |
Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
Strength | 10 |
Strength Unit | mg/1 |
Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |