NDC Code | 63739-531-10 |
Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-531-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
Product NDC | 63739-531 |
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 | 20070228 |
End Marketing Date | 20210731 |
Marketing Category Name | ANDA |
Application Number | ANDA077797 |
Manufacturer | McKesson Corporation dba SKY Packaging |
Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
Strength | 10 |
Strength Unit | mg/1 |
Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |