| NDC Code | 51991-797-98 |
|---|
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (51991-797-98) > 50 mL in 1 VIAL, SINGLE-DOSE |
|---|
| Product NDC | 51991-797 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Azacitidine |
|---|
| Non-Proprietary Name | Azacitidine |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | SUBCUTANEOUS |
|---|
| Start Marketing Date | 20170623 |
|---|
| End Marketing Date | 20240131 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207234 |
|---|
| Manufacturer | Breckenridge Pharmaceutical, Inc. |
|---|
| Substance Name | AZACITIDINE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/50mL |
|---|
| Pharmacy Classes | Nucleic Acid Synthesis Inhibitors [MoA], Nucleoside Metabolic Inhibitor [EPC] |
|---|