OPTIMARK - 0019-1177-08 - (GADOVERSETAMIDE)

Alphabetical Index


Drug Information of OPTIMARK

Product NDC: 0019-1177
Proprietary Name: OPTIMARK
Non Proprietary Name: GADOVERSETAMIDE
Active Ingredient(s): .5    mmol/mL & nbsp;   GADOVERSETAMIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of OPTIMARK

Product NDC: 0019-1177
Labeler Name: Mallinckrodt Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020975
Marketing Category: NDA
Start Marketing Date: 20101210

Package Information of OPTIMARK

Package NDC: 0019-1177-08
Package Description: 10 VIAL, GLASS in 1 CARTON (0019-1177-08) > 20 mL in 1 VIAL, GLASS

NDC Information of OPTIMARK

NDC Code 0019-1177-08
Proprietary Name OPTIMARK
Package Description 10 VIAL, GLASS in 1 CARTON (0019-1177-08) > 20 mL in 1 VIAL, GLASS
Product NDC 0019-1177
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GADOVERSETAMIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20101210
Marketing Category Name NDA
Labeler Name Mallinckrodt Inc.
Substance Name GADOVERSETAMIDE
Strength Number .5
Strength Unit mmol/mL
Pharmaceutical Classes

Complete Information of OPTIMARK


General Information