Uroxatral (Page 6 of 6)

PRINCIPAL DISPLAY PANEL — 30 TABLETS BOTTLE

30-count-tablets
(click image for full-size original)

NDC 59212-200-30


Uroxatral®
alfuzosin HCl 10 mg
Extended-Release Tablets

SWALLOW TABLET WHOLE.
DO NOT CHEW OR CRUSH TABLETS.
CONCORDIA PHARMACEUTICALS30 Tablets Rx only

PRINCIPAL DISPLAY PANEL — 100 TABLETS BOTTLE

100-count-tablets
(click image for full-size original)

NDC 59212-200-10

Uroxatral ®
alfuzosin HCl 10 mg
Extended-Release Tablets

SWALLOW TABLET WHOLE.
DO NOT CHEW OR CRUSH TABLETS.

CONCORDIA PHARMACEUTICALS 100 Tablets Rx only

UROXATRAL alfuzosin hcl tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:59212-200
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
alfuzosin hydrochloride (alfuzosin) alfuzosin hydrochloride 10 mg
Inactive Ingredients
Ingredient Name Strength
silicon dioxide
ethylcellulose (100 mpa.s)
hydrogenated castor oil
hypromelloses
magnesium stearate
mannitol
cellulose, microcrystalline
POVIDONE, UNSPECIFIED
ferric oxide yellow
Product Characteristics
Color WHITE Score no score
Shape ROUND Size 8mm
Flavor Imprint Code X10
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:59212-200-10 100 TABLET, EXTENDED RELEASE in 1 BOTTLE None
2 NDC:59212-200-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA021287 06/03/2013
Labeler — Concordia Pharmaceuticals Inc. (815240092)

Revised: 08/2021 Concordia Pharmaceuticals Inc.

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