NDC Code | 71085-010-01 |
Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (71085-010-01) |
Product NDC | 71085-010 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Cyclobenzaprine Hydrochloride |
Non-Proprietary Name | Cyclobenzaprine Hydrochloride |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20170801 |
Marketing Category Name | ANDA |
Application Number | ANDA078722 |
Manufacturer | IPG PHARMACEUTICALS, INC. |
Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
Strength | 7.5 |
Strength Unit | mg/1 |
Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |