Ultravist - 50419-342-10 - (iopromide)

Alphabetical Index


Drug Information of Ultravist

Product NDC: 50419-342
Proprietary Name: Ultravist
Non Proprietary Name: iopromide
Active Ingredient(s): 498.72    mg/mL & nbsp;   iopromide
Administration Route(s): INTRA-ARTERIAL
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ultravist

Product NDC: 50419-342
Labeler Name: Bayer HealthCare Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021425
Marketing Category: NDA
Start Marketing Date: 20091230

Package Information of Ultravist

Package NDC: 50419-342-10
Package Description: 10 VIAL, GLASS in 1 CARTON (50419-342-10) > 100 mL in 1 VIAL, GLASS

NDC Information of Ultravist

NDC Code 50419-342-10
Proprietary Name Ultravist
Package Description 10 VIAL, GLASS in 1 CARTON (50419-342-10) > 100 mL in 1 VIAL, GLASS
Product NDC 50419-342
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name iopromide
Dosage Form Name INJECTION
Route Name INTRA-ARTERIAL
Start Marketing Date 20091230
Marketing Category Name NDA
Labeler Name Bayer HealthCare Pharmaceuticals Inc.
Substance Name IOPROMIDE
Strength Number 498.72
Strength Unit mg/mL
Pharmaceutical Classes Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]

Complete Information of Ultravist


General Information