Alfuzosin hydrochloride (Liberty Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Alfuzosin hydrochloride drug offered from Liberty Pharmaceuticals, Inc.. This Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Liberty Pharmaceuticals, Inc. |
| NON-PROPRIETARY NAME: | Alfuzosin hydrochloride |
| SUBSTANCE NAME: | ALFUZOSIN HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, EXTENDED RELEASE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2012-10-02 |
| END MARKETING DATE: | 0000-00-00 |
Alfuzosin hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Alfuzosin hydrochloride from Liberty Pharmaceuticals, Inc. |
| LABELER NAME: | Liberty Pharmaceuticals, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(mg/1) |
| START MARKETING DATE: | 2012-10-02 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0440-5000_a588f193-6be7-4048-bb99-970d8925c760 |
| PRODUCT NDC: | 0440-5000 |
| APPLICATION NUMBER: | ANDA090284 |
Other ALFUZOSIN HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
