NDC 84386-153 – Alfuzosin Hydrochloride

Alfuzosin Hydrochloride 10 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC84386-153

Product details

Brand name
Alfuzosin Hydrochloride
Generic name
Alfuzosin Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA079060
Marketed since
July 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Alfuzosin Hydrochloride →

Package NDC codes (5)

Package NDCDescriptionSince
84386-153-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (84386-153-01)Jul 1, 2026
84386-153-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (84386-153-05)Jul 1, 2026
84386-153-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (84386-153-30)Jul 1, 2026
84386-153-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (84386-153-90)Jul 1, 2026
84386-153-991000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (84386-153-99)Jul 1, 2026

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