Sodium Lactate (Hospira, Inc.)
Welcome to the PulseAid listing for the Sodium Lactate 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: | SODIUM LACTATE |
SUBSTANCE NAME: | SODIUM LACTATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION, CONCENTRATE |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2006-06-28 |
END MARKETING DATE: | 0000-00-00 |
Sodium Lactate HUMAN PRESCRIPTION DRUG Details:
Item Description | Sodium Lactate from Hospira, Inc. |
LABELER NAME: | Hospira, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5.6(g/10mL) |
START MARKETING DATE: | 2006-06-28 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0409-6664_3acebc84-6521-4fe2-a9a2-52c2b2cb2b26 |
PRODUCT NDC: | 0409-6664 |
APPLICATION NUMBER: | NDA018947 |
Other SODIUM LACTATE Pharmaceutical Manufacturers / Labelers: