Dexmedetomidine Hydrochloride (Sun Pharmaceuticals Industries, Inc.)
Welcome to the PulseAid listing for the Dexmedetomidine Hydrochloride drug offered from Sun Pharmaceuticals Industries, Inc.. This Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC],General Anesthesia [PE] 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 Pharmaceuticals Industries, Inc. |
| NON-PROPRIETARY NAME: | DEXMEDETOMIDINE HYDROCHLORIDE |
| SUBSTANCE NAME: | DEXMEDETOMIDINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC],General Anesthesia [PE] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2015-04-08 |
| END MARKETING DATE: | 0000-00-00 |
Dexmedetomidine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Dexmedetomidine Hydrochloride from Sun Pharmaceuticals Industries, Inc. |
| LABELER NAME: | Sun Pharmaceuticals Industries, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 100(ug/mL) |
| START MARKETING DATE: | 2015-04-08 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 57664-596_f1113456-7fa7-4233-9b36-8b11dc911636 |
| PRODUCT NDC: | 57664-596 |
| APPLICATION NUMBER: | ANDA202126 |
Other DEXMEDETOMIDINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
