CHROMIUM - 0409-4093-01 - (CHROMIC CHLORIDE)

Alphabetical Index


Drug Information of CHROMIUM

Product NDC: 0409-4093
Proprietary Name: CHROMIUM
Non Proprietary Name: CHROMIC CHLORIDE
Active Ingredient(s): 4    ug/mL & nbsp;   CHROMIC CHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of CHROMIUM

Product NDC: 0409-4093
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018961
Marketing Category: NDA
Start Marketing Date: 20110811

Package Information of CHROMIUM

Package NDC: 0409-4093-01
Package Description: 1 TRAY in 1 CASE (0409-4093-01) > 25 VIAL, PLASTIC in 1 TRAY > 10 mL in 1 VIAL, PLASTIC

NDC Information of CHROMIUM

NDC Code 0409-4093-01
Proprietary Name CHROMIUM
Package Description 1 TRAY in 1 CASE (0409-4093-01) > 25 VIAL, PLASTIC in 1 TRAY > 10 mL in 1 VIAL, PLASTIC
Product NDC 0409-4093
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CHROMIC CHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110811
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name CHROMIC CHLORIDE
Strength Number 4
Strength Unit ug/mL
Pharmaceutical Classes Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient]

Complete Information of CHROMIUM


General Information