Anagrelide Hydrochloride (Teva Pharmaceuticals USA, Inc)
Welcome to the PulseAid listing for the Anagrelide Hydrochloride drug offered from Teva Pharmaceuticals USA, Inc. This Decreased Platelet Production [PE],Platelet-reducing Agent [EPC],Phosphodiesterase 3 Inhibitors [MoA] 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: | Teva Pharmaceuticals USA, Inc |
| NON-PROPRIETARY NAME: | Anagrelide Hydrochloride |
| SUBSTANCE NAME: | ANAGRELIDE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Decreased Platelet Production [PE],Platelet-reducing Agent [EPC],Phosphodiesterase 3 Inhibitors [MoA] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2005-04-18 |
| END MARKETING DATE: | 0000-00-00 |
Anagrelide Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Anagrelide Hydrochloride from Teva Pharmaceuticals USA, Inc |
| LABELER NAME: | Teva Pharmaceuticals USA, Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1(mg/1) |
| START MARKETING DATE: | 2005-04-18 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0172-5240_56ae5267-4bc1-4420-94a0-75df1567ca68 |
| PRODUCT NDC: | 0172-5240 |
| APPLICATION NUMBER: | ANDA076468 |
Other ANAGRELIDE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
