Calcium Gluconate (Fresenius Kabi USA, LLC)
Welcome to the PulseAid listing for the Calcium Gluconate drug offered from Fresenius Kabi USA, LLC. This Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [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: | Fresenius Kabi USA, LLC |
NON-PROPRIETARY NAME: | Calcium Gluconate |
SUBSTANCE NAME: | CALCIUM GLUCONATE MONOHYDRATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2017-06-15 |
END MARKETING DATE: | 0000-00-00 |
Calcium Gluconate HUMAN PRESCRIPTION DRUG Details:
Item Description | Calcium Gluconate from Fresenius Kabi USA, LLC |
LABELER NAME: | Fresenius Kabi USA, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 98(mg/mL) |
START MARKETING DATE: | 2017-06-15 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63323-360_8b77c3d2-992d-4261-8421-9cfd07328fbf |
PRODUCT NDC: | 63323-360 |
APPLICATION NUMBER: | NDA208418 |
Other CALCIUM GLUCONATE MONOHYDRATE Pharmaceutical Manufacturers / Labelers: