Adenosine - 63323-651-02 - (ADENOSINE)

Alphabetical Index


Drug Information of Adenosine

Product NDC: 63323-651
Proprietary Name: Adenosine
Non Proprietary Name: ADENOSINE
Active Ingredient(s): 3    mg/mL & nbsp;   ADENOSINE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Adenosine

Product NDC: 63323-651
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077133
Marketing Category: ANDA
Start Marketing Date: 20051123

Package Information of Adenosine

Package NDC: 63323-651-02
Package Description: 10 VIAL, SINGLE-USE in 1 TRAY (63323-651-02) > 2 mL in 1 VIAL, SINGLE-USE

NDC Information of Adenosine

NDC Code 63323-651-02
Proprietary Name Adenosine
Package Description 10 VIAL, SINGLE-USE in 1 TRAY (63323-651-02) > 2 mL in 1 VIAL, SINGLE-USE
Product NDC 63323-651
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ADENOSINE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20051123
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
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