NDC Code | 51655-592-54 |
Package Description | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-54) |
Product NDC | 51655-592 |
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 | 20230103 |
Marketing Category Name | ANDA |
Application Number | ANDA208170 |
Manufacturer | Northwind Pharmaceuticals, LLC |
Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
Strength | 10 |
Strength Unit | mg/1 |
Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |