COPPER - 0409-4092-01 - (CUPRIC CHLORIDE)

Alphabetical Index


Drug Information of COPPER

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)

Labeler Information of COPPER

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 Information of COPPER

Package NDC: 0409-4092-01
Package Description: 25 VIAL, PLASTIC in 1 TRAY (0409-4092-01) > 10 mL in 1 VIAL, PLASTIC

NDC Information of COPPER

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]

Complete Information of COPPER


General Information