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Cardura
Cardura - 0049-2750-41 - (doxazosin mesylate)
Drug Information of Cardura
| Product NDC: | 0049-2750 |
| Proprietary Name: | Cardura |
| Non Proprietary Name: | doxazosin mesylate |
| Active Ingredient(s): | 1 mg/1 & nbsp; doxazosin mesylate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cardura
| Product NDC: | 0049-2750 |
| Labeler Name: | Roerig |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019668 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19901102 |
Package Information of Cardura
| Package NDC: | 0049-2750-41 |
| Package Description: | 100 TABLET in 1 PACKAGE (0049-2750-41) |
NDC Information of Cardura
| NDC Code | 0049-2750-41 |
| Proprietary Name | Cardura |
| Package Description | 100 TABLET in 1 PACKAGE (0049-2750-41) |
| Product NDC | 0049-2750 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | doxazosin mesylate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19901102 |
| Marketing Category Name | NDA |
| Labeler Name | Roerig |
| Substance Name | DOXAZOSIN MESYLATE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
