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Calcium Gluconate - 0517-3950-25 - (Calcium Gluconate)

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Drug Information of Calcium Gluconate

Product NDC: 0517-3950
Proprietary Name: Calcium Gluconate
Non Proprietary Name: Calcium Gluconate
Active Ingredient(s): 98    mg/mL & nbsp;   Calcium Gluconate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Calcium Gluconate

Product NDC: 0517-3950
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19900930

Package Information of Calcium Gluconate

Package NDC: 0517-3950-25
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-3950-25) > 50 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Calcium Gluconate

NDC Code 0517-3950-25
Proprietary Name Calcium Gluconate
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-3950-25) > 50 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0517-3950
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Calcium Gluconate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19900930
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name American Regent, Inc.
Substance Name CALCIUM GLUCONATE MONOHYDRATE
Strength Number 98
Strength Unit mg/mL
Pharmaceutical Classes Calcium [Chemical/Ingredient],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA]

Complete Information of Calcium Gluconate


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