Argatroban - 0781-3285-12 - (Argatroban)

Alphabetical Index


Drug Information of Argatroban

Product NDC: 0781-3285
Proprietary Name: Argatroban
Non Proprietary Name: Argatroban
Active Ingredient(s): 125    mg/125mL & nbsp;   Argatroban
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Argatroban

Product NDC: 0781-3285
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022485
Marketing Category: NDA
Start Marketing Date: 20110509

Package Information of Argatroban

Package NDC: 0781-3285-12
Package Description: 2 VIAL, SINGLE-USE in 1 CARTON (0781-3285-12) > 125 mL in 1 VIAL, SINGLE-USE (0781-3285-54)

NDC Information of Argatroban

NDC Code 0781-3285-12
Proprietary Name Argatroban
Package Description 2 VIAL, SINGLE-USE in 1 CARTON (0781-3285-12) > 125 mL in 1 VIAL, SINGLE-USE (0781-3285-54)
Product NDC 0781-3285
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Argatroban
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110509
Marketing Category Name NDA
Labeler Name Sandoz Inc
Substance Name ARGATROBAN
Strength Number 125
Strength Unit mg/125mL
Pharmaceutical Classes Anti-coagulant [EPC],Direct Thrombin Inhibitor [EPC],Thrombin Inhibitors [MoA]

Complete Information of Argatroban


General Information