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: | NASAL |
DOSAGE FORM: | SPRAY, METERED |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2012-05-24 |
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: | 137(ug/1) |
START MARKETING DATE: | 2012-05-24 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 47335-779_540d2e65-b32c-4f73-b76b-f034a19aa1d3 |
PRODUCT NDC: | 47335-779 |
APPLICATION NUMBER: | ANDA090423 |
Other AZELASTINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: