Dextrose (Becton Dickinson and Company)
Welcome to the PulseAid listing for the Dextrose drug offered from Becton Dickinson and Company. This 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: | Becton Dickinson and Company |
| NON-PROPRIETARY NAME: | Dextrose Monohydrate |
| SUBSTANCE NAME: | DEXTROSE MONOHYDRATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-10-21 |
| END MARKETING DATE: | 0000-00-00 |
Dextrose HUMAN PRESCRIPTION DRUG Details:
| Item Description | Dextrose from Becton Dickinson and Company |
| LABELER NAME: | Becton Dickinson and Company |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 50(mg/mL) |
| START MARKETING DATE: | 2016-10-21 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 17271-720_a3afd51d-b0e4-4ee4-83f5-eb63f9d5e840 |
| PRODUCT NDC: | 17271-720 |
| APPLICATION NUMBER: | ANDA207449 |
Other DEXTROSE MONOHYDRATE Pharmaceutical Manufacturers / Labelers:
