Angiomax - 55154-2275-5 - (bivalirudin)

Alphabetical Index


Drug Information of Angiomax

Product NDC: 55154-2275
Proprietary Name: Angiomax
Non Proprietary Name: bivalirudin
Active Ingredient(s): 250    mg/1 & nbsp;   bivalirudin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Angiomax

Product NDC: 55154-2275
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020873
Marketing Category: NDA
Start Marketing Date: 20001215

Package Information of Angiomax

Package NDC: 55154-2275-5
Package Description: 5 VIAL, SINGLE-USE in 1 BAG (55154-2275-5) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE

NDC Information of Angiomax

NDC Code 55154-2275-5
Proprietary Name Angiomax
Package Description 5 VIAL, SINGLE-USE in 1 BAG (55154-2275-5) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE
Product NDC 55154-2275
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bivalirudin
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20001215
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name BIVALIRUDIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Anti-coagulant [EPC],Direct Thrombin Inhibitor [EPC],Thrombin Inhibitors [MoA]

Complete Information of Angiomax


General Information