Alfuzosin Hydrochloride
- Strength
- 10 mg/1
- Form
- Tablet, Extended Release
- Class
- alpha-Adrenergic Blocker
Sun Pharmaceutical Industries, Inc.
Listed by Aurobindo Pharma Limited
| Dosage form | Tablet, Film Coated, Extended Release |
|---|---|
| Route | Oral |
| Drug class | alpha-Adrenergic Blocker |
| Approval route | ANDA — approved generic |
| NDC code | 65862-249 |
| FDA application | ANDA079060 |
| RxNorm concept | 861132 |
| Package sizes listed | 5 |
| Marketed since | August 2012 |
Same active ingredient, different manufacturer, strength or form. Products matching on both ingredient and strength are usually interchangeable — but confirm before switching, especially with modified-release forms.
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Information only, not medical advice. Nothing on this page indicates that a medication is safe or suitable for you. Speak to a prescriber or pharmacist before starting, stopping or switching any medicine.
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