Dextrose (Hospira, Inc.)
Welcome to the PulseAid listing for the Dextrose drug offered from Hospira, Inc.. 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: | Hospira, Inc. |
| NON-PROPRIETARY NAME: | DEXTROSE MONOHYDRATE |
| SUBSTANCE NAME: | DEXTROSE MONOHYDRATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2005-12-07 |
| END MARKETING DATE: | 0000-00-00 |
Dextrose HUMAN PRESCRIPTION DRUG Details:
| Item Description | Dextrose from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 25(g/50mL) |
| START MARKETING DATE: | 2005-12-07 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-4902_e44eac3c-b53c-4f84-a55f-21c419b3ac0f |
| PRODUCT NDC: | 0409-4902 |
| APPLICATION NUMBER: | |
Other DEXTROSE MONOHYDRATE Pharmaceutical Manufacturers / Labelers:
