Product NDC: | 35356-662 |
Proprietary Name: | TIZANIDINE HYDROCHLORIDE |
Non Proprietary Name: | TIZANIDINE HYDROCHLORIDE |
Active Ingredient(s): | 2 mg/1 & nbsp; TIZANIDINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-662 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076347 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070206 |
Package NDC: | 35356-662-60 |
Package Description: | 60 TABLET in 1 BOTTLE (35356-662-60) |
NDC Code | 35356-662-60 |
Proprietary Name | TIZANIDINE HYDROCHLORIDE |
Package Description | 60 TABLET in 1 BOTTLE (35356-662-60) |
Product NDC | 35356-662 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | TIZANIDINE HYDROCHLORIDE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20070206 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | TIZANIDINE HYDROCHLORIDE |
Strength Number | 2 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |