| Product NDC: | 25021-301 | 
| 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) | 
| Product NDC: | 25021-301 | 
| Labeler Name: | Sagent Pharmaceuticals, Inc | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA077283 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20071201 | 
| Package NDC: | 25021-301-76 | 
| Package Description: | 10 CARTON in 1 BOX (25021-301-76) > 1 SYRINGE in 1 CARTON > 4 mL in 1 SYRINGE | 
| NDC Code | 25021-301-76 | 
| Proprietary Name | Adenosine | 
| Package Description | 10 CARTON in 1 BOX (25021-301-76) > 1 SYRINGE in 1 CARTON > 4 mL in 1 SYRINGE | 
| Product NDC | 25021-301 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Adenosine | 
| Dosage Form Name | INJECTION | 
| Route Name | INTRAVENOUS | 
| Start Marketing Date | 20071201 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Sagent Pharmaceuticals, Inc | 
| Substance Name | ADENOSINE | 
| Strength Number | 3 | 
| Strength Unit | mg/mL | 
| Pharmaceutical Classes | Adenosine Receptor Agonist [EPC],Adenosine Receptor Agonists [MoA] |