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Alfuzosin Hydrochloride
Alfuzosin Hydrochloride - 47335-956-18 - (Alfuzosin Hydrochloride)
Drug Information of Alfuzosin Hydrochloride
| Product NDC: | 47335-956 |
| 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: | 47335-956 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079057 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111122 |
Package Information of Alfuzosin Hydrochloride
| Package NDC: | 47335-956-18 |
| Package Description: | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-18) |
NDC Information of Alfuzosin Hydrochloride
| NDC Code | 47335-956-18 |
| Proprietary Name | Alfuzosin Hydrochloride |
| Package Description | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-18) |
| Product NDC | 47335-956 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Alfuzosin Hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20111122 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | ALFUZOSIN HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
