Azelastine Hydrochloride (Sun Pharma Global FZE)
Welcome to the PulseAid listing for the Azelastine Hydrochloride drug offered from Sun Pharma Global FZE. This Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [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: | Sun Pharma Global FZE |
| NON-PROPRIETARY NAME: | Azelastine Hydrochloride |
| SUBSTANCE NAME: | AZELASTINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
| ROUTE: | INTRAOCULAR |
| DOSAGE FORM: | SOLUTION/ DROPS |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2010-05-31 |
| END MARKETING DATE: | 0000-00-00 |
Azelastine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Azelastine Hydrochloride from Sun Pharma Global FZE |
| LABELER NAME: | Sun Pharma Global FZE |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 0.5(mg/mL) |
| START MARKETING DATE: | 2010-05-31 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 47335-938_81e4a7c3-5448-47d2-bdf8-daa851be2387 |
| PRODUCT NDC: | 47335-938 |
| APPLICATION NUMBER: | ANDA078738 |
Other AZELASTINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
