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Calcium Gluconate - 63323-311-61 - (CALCIUM GLUCONATE)

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Drug Information of Calcium Gluconate

Product NDC: 63323-311
Proprietary Name: Calcium Gluconate
Non Proprietary Name: CALCIUM GLUCONATE
Active Ingredient(s): 94    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: 63323-311
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20000712

Package Information of Calcium Gluconate

Package NDC: 63323-311-61
Package Description: 20 VIAL in 1 TRAY (63323-311-61) > 100 mL in 1 VIAL

NDC Information of Calcium Gluconate

NDC Code 63323-311-61
Proprietary Name Calcium Gluconate
Package Description 20 VIAL in 1 TRAY (63323-311-61) > 100 mL in 1 VIAL
Product NDC 63323-311
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CALCIUM GLUCONATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20000712
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name APP Pharmaceuticals, LLC
Substance Name CALCIUM GLUCONATE
Strength Number 94
Strength Unit mg/mL
Pharmaceutical Classes Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient]

Complete Information of Calcium Gluconate


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