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