ALFUZOSIN HYDROCHLORIDE is a Oral Tablet, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Torrent Pharmaceuticals Limited. The primary component is Alfuzosin Hydrochloride.
| Product ID | 13668-021_3cea1b49-3f10-4090-9ade-765a798f1443 | 
| NDC | 13668-021 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | ALFUZOSIN HYDROCHLORIDE | 
| Generic Name | Alfuzosin Hydrochloride | 
| Dosage Form | Tablet, Extended Release | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2011-07-18 | 
| Marketing Category | ANDA / ANDA | 
| Application Number | ANDA079054 | 
| Labeler Name | Torrent Pharmaceuticals Limited | 
| Substance Name | ALFUZOSIN HYDROCHLORIDE | 
| Active Ingredient Strength | 10 mg/1 | 
| Pharm Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2019-12-31 | 
| Marketing Start Date | 2011-07-18 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | ANDA | 
| Application Number | ANDA079054 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2011-07-18 | 
| Marketing End Date | 2021-10-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA079054 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2011-07-18 | 
| Marketing End Date | 2021-10-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA079054 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2011-07-18 | 
| Marketing End Date | 2021-10-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA079054 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2011-07-18 | 
| Marketing End Date | 2021-10-31 | 
| Ingredient | Strength | 
|---|---|
| ALFUZOSIN HYDROCHLORIDE | 10 mg/1 | 
| SPL SET ID: | 6220496a-b651-4e7b-9a41-0ea949de3df0 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0378-5005 | Alfuzosin Hydrochloride | alfuzosin | 
| 0440-5000 | Alfuzosin hydrochloride | Alfuzosin hydrochloride | 
| 13668-021 | ALFUZOSIN HYDROCHLORIDE | ALFUZOSIN HYDROCHLORIDE | 
| 29300-155 | Alfuzosin hydrochloride | Alfuzosin hydrochloride | 
| 31722-302 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 33261-994 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 42291-110 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 43353-746 | Alfuzosin Hydrochloride | alfuzosin | 
| 43353-945 | Alfuzosin hydrochloride | Alfuzosin hydrochloride | 
| 47335-956 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 55648-738 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 57237-114 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 60505-2850 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 61919-349 | ALFUZOSIN HYDROCHLORIDE | ALFUZOSIN HYDROCHLORIDE | 
| 63629-2353 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 63629-2354 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 63629-7907 | Alfuzosin hydrochloride | Alfuzosin hydrochloride | 
| 63629-9155 | Alfuzosin hydrochloride | Alfuzosin hydrochloride | 
| 63629-9295 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 64679-738 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 65862-249 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 69097-844 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 70934-306 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 70934-961 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride | 
| 76282-302 | Alfuzosin hydrochloride | Alfuzosin hydrochloride | 
| 71335-1529 | Alfuzosin Hydrochloride | Alfuzosin Hydrochloride |