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Uroxatral
Uroxatral - 0024-4200-10 - (alfuzosin hydrochloride)
Drug Information of Uroxatral
| Product NDC: | 0024-4200 |
| Proprietary Name: | Uroxatral |
| Non Proprietary Name: | alfuzosin hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; alfuzosin hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Uroxatral
| Product NDC: | 0024-4200 |
| Labeler Name: | sanofi-aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021287 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090605 |
Package Information of Uroxatral
| Package NDC: | 0024-4200-10 |
| Package Description: | 1 BOTTLE in 1 CARTON (0024-4200-10) > 100 TABLET, EXTENDED RELEASE in 1 BOTTLE |
NDC Information of Uroxatral
| NDC Code | 0024-4200-10 |
| Proprietary Name | Uroxatral |
| Package Description | 1 BOTTLE in 1 CARTON (0024-4200-10) > 100 TABLET, EXTENDED RELEASE in 1 BOTTLE |
| Product NDC | 0024-4200 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | alfuzosin hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090605 |
| Marketing Category Name | NDA |
| Labeler Name | sanofi-aventis U.S. LLC |
| Substance Name | ALFUZOSIN HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
