Peditrace - 63323-147-10 - (ZINC, COPPER, MANGANESE, SELENIUM, FLUORINE, and IODINE)

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Drug Information of Peditrace

Product NDC: 63323-147
Proprietary Name: Peditrace
Non Proprietary Name: ZINC, COPPER, MANGANESE, SELENIUM, FLUORINE, and IODINE
Active Ingredient(s): 20; 1; 1; 57; 2; 250    ug/mL; ug/mL; ug/mL; ug/mL; ug/mL; ug/mL & nbsp;   ZINC, COPPER, MANGANESE, SELENIUM, FLUORINE, and IODINE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Peditrace

Product NDC: 63323-147
Labeler Name: Fresenius Kabi USA, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Start Marketing Date: 20130509

Package Information of Peditrace

Package NDC: 63323-147-10
Package Description: 10 VIAL, PLASTIC in 1 CARTON (63323-147-10) > 10 mL in 1 VIAL, PLASTIC

NDC Information of Peditrace

NDC Code 63323-147-10
Proprietary Name Peditrace
Package Description 10 VIAL, PLASTIC in 1 CARTON (63323-147-10) > 10 mL in 1 VIAL, PLASTIC
Product NDC 63323-147
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ZINC, COPPER, MANGANESE, SELENIUM, FLUORINE, and IODINE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20130509
Marketing Category Name UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Labeler Name Fresenius Kabi USA, LLC
Substance Name CUPRIC CHLORIDE; MANGANESE CHLORIDE; POTASSIUM IODIDE; SODIUM FLUORIDE; SODIUM SELENITE; ZINC CHLORIDE
Strength Number 20; 1; 1; 57; 2; 250
Strength Unit ug/mL; ug/mL; ug/mL; ug/mL; ug/mL; ug/mL
Pharmaceutical Classes Copper Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE],Magnetic Resonance Contrast Activity [MoA],Paramagnetic Contrast Agent [EPC]

Complete Information of Peditrace


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