HETASTARCH IN SODIUM CHLORIDE (Hospira, Inc.)
Welcome to the PulseAid listing for the HETASTARCH IN SODIUM CHLORIDE drug offered from Hospira, Inc.. This Plasma Volume Expander [EPC],Increased Intravascular Volume [PE],Osmotic Activity [MoA],Starch [Chemical/Ingredient] 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: | HETASTARCH |
| SUBSTANCE NAME: | HETASTARCH |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Plasma Volume Expander [EPC],Increased Intravascular Volume [PE],Osmotic Activity [MoA],Starch [Chemical/Ingredient] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2005-05-26 |
| END MARKETING DATE: | 0000-00-00 |
HETASTARCH IN SODIUM CHLORIDE HUMAN PRESCRIPTION DRUG Details:
| Item Description | HETASTARCH IN SODIUM CHLORIDE from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 6(g/100mL) |
| START MARKETING DATE: | 2005-05-26 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-7248_25e5dcb2-4a6b-4d84-b4f1-da17f0931bff |
| PRODUCT NDC: | 0409-7248 |
| APPLICATION NUMBER: | BA740193 |
Other HETASTARCH Pharmaceutical Manufacturers / Labelers:
