Product NDC: | 35356-717 |
Proprietary Name: | cyclobenzaprine hydrochloride |
Non Proprietary Name: | cyclobenzaprine hydrochloride |
Active Ingredient(s): | 10 mg/1 & nbsp; cyclobenzaprine hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-717 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077563 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100423 |
Package NDC: | 35356-717-90 |
Package Description: | 90 TABLET in 1 BOTTLE (35356-717-90) |
NDC Code | 35356-717-90 |
Proprietary Name | cyclobenzaprine hydrochloride |
Package Description | 90 TABLET in 1 BOTTLE (35356-717-90) |
Product NDC | 35356-717 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | cyclobenzaprine hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100423 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | CYCLOBENZAPRINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |