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Adenoscan
Adenoscan - 49349-758-01 - (adenosine)
Drug Information of Adenoscan
| Product NDC: | 49349-758 |
| Proprietary Name: | Adenoscan |
| Non Proprietary Name: | adenosine |
| Active Ingredient(s): | 3 mg/mL & nbsp; adenosine |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Adenoscan
| Product NDC: | 49349-758 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020059 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130627 |
Package Information of Adenoscan
| Package NDC: | 49349-758-01 |
| Package Description: | 20 mL in 1 VIAL (49349-758-01) |
NDC Information of Adenoscan
| NDC Code | 49349-758-01 |
| Proprietary Name | Adenoscan |
| Package Description | 20 mL in 1 VIAL (49349-758-01) |
| Product NDC | 49349-758 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | adenosine |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20130627 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | ADENOSINE |
| Strength Number | 3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adenosine Receptor Agonist [EPC],Adenosine Receptor Agonists [MoA] |
