Optiray - 0019-1323-11 - (Ioversol)

Alphabetical Index


Drug Information of Optiray

Product NDC: 0019-1323
Proprietary Name: Optiray
Non Proprietary Name: Ioversol
Active Ingredient(s): 678    mg/mL & nbsp;   Ioversol
Administration Route(s): INTRA-ARTERIAL; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Optiray

Product NDC: 0019-1323
Labeler Name: Mallinckrodt Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019710
Marketing Category: NDA
Start Marketing Date: 20120304

Package Information of Optiray

Package NDC: 0019-1323-11
Package Description: 12 BOTTLE, GLASS in 1 CARTON (0019-1323-11) > 100 mL in 1 BOTTLE, GLASS

NDC Information of Optiray

NDC Code 0019-1323-11
Proprietary Name Optiray
Package Description 12 BOTTLE, GLASS in 1 CARTON (0019-1323-11) > 100 mL in 1 BOTTLE, GLASS
Product NDC 0019-1323
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ioversol
Dosage Form Name INJECTION
Route Name INTRA-ARTERIAL; INTRAVENOUS
Start Marketing Date 20120304
Marketing Category Name NDA
Labeler Name Mallinckrodt Inc.
Substance Name IOVERSOL
Strength Number 678
Strength Unit mg/mL
Pharmaceutical Classes Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]

Complete Information of Optiray


General Information