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Adenosine
Adenosine - 63323-651-04 - (ADENOSINE)
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: | 63323-651-04 |
| Package Description: | 10 VIAL, SINGLE-USE in 1 TRAY (63323-651-04) > 4 mL in 1 VIAL, SINGLE-USE |
NDC Information of Adenosine
| NDC Code | 63323-651-04 |
| Proprietary Name | Adenosine |
| Package Description | 10 VIAL, SINGLE-USE in 1 TRAY (63323-651-04) > 4 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] |
