Alfuzosin Hydrochloride 51655-0967-52

Package NDC

51655-0967-52

Manufacturer: Northwind Health Company, Llc
Dosage Form: Tablet, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 29, 2023
Listing Expires: December 31, 2027
Application: ANDA203192

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Active Ingredients

Ingredient	Strength
Alfuzosin Hydrochloride	10 mg/1

Drug Class

Adrenergic alpha-Antagonists [MoA]alpha-Adrenergic Blocker [EPC]

Selected Package

51655-0967-52Selected

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-967-52)