Product NDC: | 0409-4092 |
Proprietary Name: | COPPER |
Non Proprietary Name: | CUPRIC CHLORIDE |
Active Ingredient(s): | .4 mg/mL & nbsp; CUPRIC CHLORIDE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-4092 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018960 |
Marketing Category: | NDA |
Start Marketing Date: | 20100728 |
Package NDC: | 0409-4092-01 |
Package Description: | 25 VIAL, PLASTIC in 1 TRAY (0409-4092-01) > 10 mL in 1 VIAL, PLASTIC |
NDC Code | 0409-4092-01 |
Proprietary Name | COPPER |
Package Description | 25 VIAL, PLASTIC in 1 TRAY (0409-4092-01) > 10 mL in 1 VIAL, PLASTIC |
Product NDC | 0409-4092 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CUPRIC CHLORIDE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100728 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | CUPRIC CHLORIDE |
Strength Number | .4 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Copper [Chemical/Ingredient],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE] |