Adenosine - 17478-542-02 - (adenosine)

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Drug Information of Adenosine

Product NDC: 17478-542
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: 17478-542
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078076
Marketing Category: ANDA
Start Marketing Date: 20110317

Package Information of Adenosine

Package NDC: 17478-542-02
Package Description: 10 VIAL in 1 CARTON (17478-542-02) > 2 mL in 1 VIAL

NDC Information of Adenosine

NDC Code 17478-542-02
Proprietary Name Adenosine
Package Description 10 VIAL in 1 CARTON (17478-542-02) > 2 mL in 1 VIAL
Product NDC 17478-542
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name adenosine
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110317
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
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