ADENOSINE - 55648-630-04 - (ADENOSINE)

Alphabetical Index


Drug Information of ADENOSINE

Product NDC: 55648-630
Proprietary Name: ADENOSINE
Non Proprietary Name: ADENOSINE
Active Ingredient(s): 3    mg/mL & nbsp;   ADENOSINE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of ADENOSINE

Product NDC: 55648-630
Labeler Name: WOCKHARDT LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090220
Marketing Category: ANDA
Start Marketing Date: 20090720

Package Information of ADENOSINE

Package NDC: 55648-630-04
Package Description: 1 VIAL in 1 CARTON (55648-630-04) > 30 mL in 1 VIAL

NDC Information of ADENOSINE

NDC Code 55648-630-04
Proprietary Name ADENOSINE
Package Description 1 VIAL in 1 CARTON (55648-630-04) > 30 mL in 1 VIAL
Product NDC 55648-630
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ADENOSINE
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20090720
Marketing Category Name ANDA
Labeler Name WOCKHARDT LIMITED
Substance Name ADENOSINE
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes Adenosine Receptor Agonist [EPC],Adenosine Receptor Agonists [MoA]

Complete Information of ADENOSINE


General Information