Oxilan - 67684-1001-3 - (Ioxilan Injection)

Alphabetical Index


Drug Information of Oxilan

Product NDC: 67684-1001
Proprietary Name: Oxilan
Non Proprietary Name: Ioxilan Injection
Active Ingredient(s): 350    mg/mL & nbsp;   Ioxilan Injection
Administration Route(s): INTRAVASCULAR
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Oxilan

Product NDC: 67684-1001
Labeler Name: Guerbet LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020316
Marketing Category: NDA
Start Marketing Date: 20020318

Package Information of Oxilan

Package NDC: 67684-1001-3
Package Description: 10 BOTTLE in 1 CARTON (67684-1001-3) > 150 mL in 1 BOTTLE

NDC Information of Oxilan

NDC Code 67684-1001-3
Proprietary Name Oxilan
Package Description 10 BOTTLE in 1 CARTON (67684-1001-3) > 150 mL in 1 BOTTLE
Product NDC 67684-1001
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ioxilan Injection
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVASCULAR
Start Marketing Date 20020318
Marketing Category Name NDA
Labeler Name Guerbet LLC
Substance Name IOXILAN
Strength Number 350
Strength Unit mg/mL
Pharmaceutical Classes Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]

Complete Information of Oxilan


General Information