Details for New Drug Application (NDA): 079057
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The generic ingredient in ALFUZOSIN HYDROCHLORIDE is alfuzosin hydrochloride. There are nineteen drug master file entries for this compound. Twelve suppliers are listed for this compound. Additional details are available on the alfuzosin hydrochloride profile page.
Summary for 079057
Tradename: | ALFUZOSIN HYDROCHLORIDE |
Applicant: | Sun Pharm |
Ingredient: | alfuzosin hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 079057
Mechanism of Action | Adrenergic alpha-Antagonists |
Suppliers and Packaging for NDA: 079057
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
ALFUZOSIN HYDROCHLORIDE | alfuzosin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 079057 | ANDA | Sun Pharmaceutical Industries, Inc. | 47335-956 | 47335-956-08 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-08) |
ALFUZOSIN HYDROCHLORIDE | alfuzosin hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 079057 | ANDA | Sun Pharmaceutical Industries, Inc. | 47335-956 | 47335-956-18 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-956-18) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, EXTENDED RELEASE;ORAL | Strength | 10MG | ||||
Approval Date: | Jul 18, 2011 | TE: | AB | RLD: | No |
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