NDC 69097-844 – Alfuzosin Hydrochloride extended release

Alfuzosin Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69097-844

Product details

Brand name
Alfuzosin Hydrochloride extended release
Generic name
Alfuzosin Hydrochloride
Labeler
Cipla USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090284
Marketed since
June 30, 2016
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
69097-844-0230 TABLET in 1 BOTTLE (69097-844-02)Jun 30, 2016
69097-844-0590 TABLET in 1 BOTTLE (69097-844-05)Jun 30, 2016
69097-844-07100 TABLET in 1 BOTTLE (69097-844-07)Jun 30, 2016
69097-844-12500 TABLET in 1 BOTTLE (69097-844-12)Jun 30, 2016

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