Home
>
National Drug Code (NDC)
>
Alfuzosin hydrochloride
Alfuzosin hydrochloride - 76282-302-01 - (Alfuzosin hydrochloride)
Drug Information of Alfuzosin hydrochloride
| Product NDC: | 76282-302 |
| Proprietary Name: | Alfuzosin hydrochloride |
| 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 Alfuzosin hydrochloride
| Product NDC: | 76282-302 |
| Labeler Name: | Exelan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090284 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121002 |
Package Information of Alfuzosin hydrochloride
| Package NDC: | 76282-302-01 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-01) |
NDC Information of Alfuzosin hydrochloride
| NDC Code | 76282-302-01 |
| Proprietary Name | Alfuzosin hydrochloride |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-302-01) |
| Product NDC | 76282-302 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Alfuzosin hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20121002 |
| Marketing Category Name | ANDA |
| Labeler Name | Exelan Pharmaceuticals Inc. |
| Substance Name | ALFUZOSIN HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
