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