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ALFUZOSIN HYDROCHLORIDE
ALFUZOSIN HYDROCHLORIDE - 13668-021-01 - (ALFUZOSIN HYDROCHLORIDE)
Drug Information of ALFUZOSIN HYDROCHLORIDE
| Product NDC: | 13668-021 |
| 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: | 13668-021 |
| Labeler Name: | Torrent Pharmaceuticals Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079054 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110718 |
Package Information of ALFUZOSIN HYDROCHLORIDE
| Package NDC: | 13668-021-01 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-021-01) |
NDC Information of ALFUZOSIN HYDROCHLORIDE
| NDC Code | 13668-021-01 |
| Proprietary Name | ALFUZOSIN HYDROCHLORIDE |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-021-01) |
| Product NDC | 13668-021 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ALFUZOSIN HYDROCHLORIDE |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110718 |
| Marketing Category Name | ANDA |
| Labeler Name | Torrent Pharmaceuticals Limited |
| Substance Name | ALFUZOSIN HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
