Strength
10 mg/1
Manufacturer
Apotex Corp.NDC
60505285009
Classification
Generic
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
ALFUZOSIN HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA079013On Market Since
9/8/2023
Pharmacological Classes
Adrenergic alpha-Antagonists
alpha-Adrenergic Blocker
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