Product NDC: | 60429-956 |
Proprietary Name: | Doxazosin mesylate |
Non Proprietary Name: | doxazosin mesylate |
Active Ingredient(s): | 8 mg/1 & nbsp; doxazosin mesylate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60429-956 |
Labeler Name: | Golden State Medical Supply, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076161 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040610 |
Package NDC: | 60429-956-10 |
Package Description: | 1000 TABLET in 1 BOTTLE (60429-956-10) |
NDC Code | 60429-956-10 |
Proprietary Name | Doxazosin mesylate |
Package Description | 1000 TABLET in 1 BOTTLE (60429-956-10) |
Product NDC | 60429-956 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | doxazosin mesylate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20040610 |
Marketing Category Name | ANDA |
Labeler Name | Golden State Medical Supply, Inc. |
Substance Name | DOXAZOSIN MESYLATE |
Strength Number | 8 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |