Dexmedetomidine Hydrochloride (Sandoz Inc)
Welcome to the PulseAid listing for the Dexmedetomidine Hydrochloride drug offered from Sandoz 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: | Sandoz 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: | 2016-11-14 |
| END MARKETING DATE: | 0000-00-00 |
Dexmedetomidine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Dexmedetomidine Hydrochloride from Sandoz Inc |
| LABELER NAME: | Sandoz Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 100(ug/mL) |
| START MARKETING DATE: | 2016-11-14 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0781-3297_e3c1f948-e7ce-4dfa-af3c-3a7f11eed6db |
| PRODUCT NDC: | 0781-3297 |
| APPLICATION NUMBER: | ANDA091465 |
Other DEXMEDETOMIDINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
