OMNIPAQUE - 0407-1411-20 - (Iohexol)

Alphabetical Index


Drug Information of OMNIPAQUE

Product NDC: 0407-1411
Proprietary Name: OMNIPAQUE
Non Proprietary Name: Iohexol
Active Ingredient(s): 388.3    mg/mL & nbsp;   Iohexol
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of OMNIPAQUE

Product NDC: 0407-1411
Labeler Name: GE Healthcare Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018956
Marketing Category: NDA
Start Marketing Date: 20040715

Package Information of OMNIPAQUE

Package NDC: 0407-1411-20
Package Description: 10 VIAL, GLASS in 1 BOX (0407-1411-20) > 20 mL in 1 VIAL, GLASS

NDC Information of OMNIPAQUE

NDC Code 0407-1411-20
Proprietary Name OMNIPAQUE
Package Description 10 VIAL, GLASS in 1 BOX (0407-1411-20) > 20 mL in 1 VIAL, GLASS
Product NDC 0407-1411
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Iohexol
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20040715
Marketing Category Name NDA
Labeler Name GE Healthcare Inc.
Substance Name IOHEXOL
Strength Number 388.3
Strength Unit mg/mL
Pharmaceutical Classes Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]

Complete Information of OMNIPAQUE


General Information