Alfuzosin Hydrochloride 51655-0087

Product NDC

51655-0087

Manufacturer: Northwind Health Company, Llc
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 4, 2022
Listing Expires: December 31, 2027
Application: ANDA079060

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Active Ingredients

Ingredient	Strength
Alfuzosin Hydrochloride	10 mg/1

Drug Class

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

Packaging Options(1)

51655-0087-52

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-087-52)

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