NDC Code | 54868-1110-5 |
Package Description | 15 TABLET in 1 BOTTLE (54868-1110-5) |
Product NDC | 54868-1110 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Cyclobenzaprine Hydrochloride |
Non-Proprietary Name | Cyclobenzaprine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 19970317 |
Marketing Category Name | ANDA |
Application Number | ANDA071611 |
Manufacturer | Physicians Total Care, Inc. |
Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
Strength | 10 |
Strength Unit | mg/1 |
Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |