Calcium Gluconate (American Regent, Inc.)


Welcome to the PulseAid listing for the Calcium Gluconate drug offered from American Regent, Inc.. This Calcium [Chemical/Ingredient],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA] 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: American Regent, Inc.
NON-PROPRIETARY NAME: Calcium Gluconate
SUBSTANCE NAME: CALCIUM GLUCONATE MONOHYDRATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Calcium [Chemical/Ingredient],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 1992-12-01
END MARKETING DATE: 0000-00-00


Calcium Gluconate HUMAN PRESCRIPTION DRUG Details:

Item DescriptionCalcium Gluconate from American Regent, Inc.
LABELER NAME: American Regent, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 98(mg/mL)
START MARKETING DATE: 1992-12-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0517-3900_5178d569-7ff6-46de-a8ce-498e9608ef3f
PRODUCT NDC: 0517-3900
APPLICATION NUMBER:

Other CALCIUM GLUCONATE MONOHYDRATE Pharmaceutical Manufacturers / Labelers:

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