Isovue - 0270-1315-98 - (IOPAMIDOL)

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Drug Information of Isovue

Product NDC: 0270-1315
Proprietary Name: Isovue
Non Proprietary Name: IOPAMIDOL
Active Ingredient(s): 612    mg/mL & nbsp;   IOPAMIDOL
Administration Route(s): INTRAVASCULAR
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Isovue

Product NDC: 0270-1315
Labeler Name: Bracco Diagnostics Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018735
Marketing Category: NDA
Start Marketing Date: 19941012

Package Information of Isovue

Package NDC: 0270-1315-98
Package Description: 6 BOTTLE in 1 BOX (0270-1315-98) > 500 mL in 1 BOTTLE

NDC Information of Isovue

NDC Code 0270-1315-98
Proprietary Name Isovue
Package Description 6 BOTTLE in 1 BOX (0270-1315-98) > 500 mL in 1 BOTTLE
Product NDC 0270-1315
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name IOPAMIDOL
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVASCULAR
Start Marketing Date 19941012
Marketing Category Name NDA
Labeler Name Bracco Diagnostics Inc
Substance Name IOPAMIDOL
Strength Number 612
Strength Unit mg/mL
Pharmaceutical Classes Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]

Complete Information of Isovue


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