Product NDC: | 54868-4767 |
Proprietary Name: | Doxazosin |
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: | 54868-4767 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075509 |
Marketing Category: | ANDA |
Start Marketing Date: | 20030403 |
Package NDC: | 54868-4767-2 |
Package Description: | 90 TABLET in 1 BOTTLE, PLASTIC (54868-4767-2) |
NDC Code | 54868-4767-2 |
Proprietary Name | Doxazosin |
Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (54868-4767-2) |
Product NDC | 54868-4767 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Doxazosin Mesylate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20030403 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | DOXAZOSIN MESYLATE |
Strength Number | 8 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |