Heparin Sodium (Hospira, Inc.)
Welcome to the PulseAid listing for the Heparin Sodium drug offered from Hospira, Inc.. This Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] 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: | HEPARIN SODIUM |
SUBSTANCE NAME: | HEPARIN SODIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |
ROUTE: | INTRAVENOUS; SUBCUTANEOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2005-02-28 |
END MARKETING DATE: | 0000-00-00 |
Heparin Sodium HUMAN PRESCRIPTION DRUG Details:
Item Description | Heparin Sodium from Hospira, Inc. |
LABELER NAME: | Hospira, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 10000([USP’U]/mL) |
START MARKETING DATE: | 2005-02-28 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0409-1316_15074707-3bd6-4bbd-9c13-0c34dc4fab9d |
PRODUCT NDC: | 0409-1316 |
APPLICATION NUMBER: | ANDA089522 |
Other HEPARIN SODIUM Pharmaceutical Manufacturers / Labelers: