Adenosine - 0641-6113-10 - (Adenosine)

Alphabetical Index


Drug Information of Adenosine

Product NDC: 0641-6113
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: 0641-6113
Labeler Name: West-ward Pharmaceutical Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076500
Marketing Category: ANDA
Start Marketing Date: 20040616

Package Information of Adenosine

Package NDC: 0641-6113-10
Package Description: 10 VIAL in 1 CARTON (0641-6113-10) > 2 mL in 1 VIAL (0641-6113-01)

NDC Information of Adenosine

NDC Code 0641-6113-10
Proprietary Name Adenosine
Package Description 10 VIAL in 1 CARTON (0641-6113-10) > 2 mL in 1 VIAL (0641-6113-01)
Product NDC 0641-6113
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Adenosine
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20040616
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp.
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