NDC Code | 60760-536-04 |
Package Description | 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-536-04) |
Product NDC | 60760-536 |
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 | 20220615 |
Marketing Category Name | ANDA |
Application Number | ANDA078643 |
Manufacturer | St Mary's Medical Park Pharmacy |
Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
Strength | 5 |
Strength Unit | mg/1 |
Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |