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 DescriptionCalcium Gluconate from Fresenius Kabi USA, LLC
LABELER NAME: Fresenius Kabi USA, LLC
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
American Regent, Inc.Calcium Gluconate
Fresenius Kabi USA, LLCCalcium Gluconate