Alfuzosin Hydrochloride Er
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Questions & Answers
Side Effects & Adverse Reactions
There is currently no warning information available for this product. We apologize for any inconvenience.
Legal Issues
There is currently no legal information available for this drug.
FDA Safety Alerts
There are currently no FDA safety alerts available for this drug.
Manufacturer Warnings
There is currently no manufacturer warning information available for this drug.
FDA Labeling Changes
There are currently no FDA labeling changes available for this drug.
Uses
Alfuzosin hydrochloride extended-release tablets, USP are indicated for the treatment of signs and symptoms of benign prostatic hyperplasia.
Alfuzosin hydrochloride extended-release tablets, USP are not indicated for the treatment of hypertension.
Alfuzosin hydrochloride extended-release tablets, USP are not indicated for use in the pediatric population.
Alfuzosin hydrochloride extended-release tablets, USP are not indicated for the treatment of hypertension.
Alfuzosin hydrochloride extended-release tablets, USP are not indicated for use in the pediatric population.
History
There is currently no drug history available for this drug.
Other Information
Each alfuzosin hydrochloride extended-release tablet, USP contains 10 mg alfuzosin hydrochloride, USP as the active ingredient. Alfuzosin hydrochloride, USP is a white to off-white powder that melts at 231° to 233°C. It is freely soluble in water, sparingly soluble in alcohol, and practically insoluble in dichloromethane.
Alfuzosin hydrochloride, USP is (R,S)-N-[3-[(4-amino-6,7-dimethoxy-2-quinazolinyl) methylamino] propyl] tetrahydro-2-furancarboxamide hydrochloride. The empirical formula of alfuzosin hydrochloride, USP is C19H27N5O4•HCl. The molecular weight of alfuzosin hydrochloride, USP is 425.92. Its structural formula is:
The tablet also contains the following inactive ingredients: dibasic calcium phosphate dihydrate (USP), hydroxypropyl methylcellulose (USP), magnesium stearate (NF), polyvinyl acetate phtalate (NF) and yellow ferric oxide (NF).
Meets USP Dissolution Test 3.
Sources
Alfuzosin Hydrochloride Er Manufacturers
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Avkare, Inc.
![Alfuzosin Hydrochloride Er (Alfuzosin Hydrochloride) Tablet, Extended Release [Avkare, Inc.]](/wp-content/themes/bootstrap/assets/img/loading2.gif)
Alfuzosin Hydrochloride Er | Avkare, Inc.
The recommended dosage is one 10 mg alfuzosin hydrochloride extended-release tablet once daily. The extent of absorption of alfuzosin is 50% lower under fasting conditions. Therefore, alfuzosin hydrochloride extended-release tablets should be taken with food and with the same meal each day. The tablets should not be chewed or crushed.
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