| NDC Code: |
53150-317 |
| Proprietary Name: |
DOXOrubicin Hydrochloride |
| Suffix: |
|
| Non-Proprietary Name: |
DOXOrubicin Hydrochloride |
| Dosage Form: |
INJECTION |
| Method: |
INTRAVENOUS |
| Original Marketing Date: |
30-04-2013 |
| Category Name: |
ANDA |
| Application Number: |
ANDA200901 |
| Labeler: |
AMNEAL AGILA, LLC |
| Substance Name: |
DOXORUBICIN HYDROCHLORIDE |
| Active Numerator Strength: |
200 |
| Active Ingredient Unit: |
mg/100mL |
| Pharm Classes: |
Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
| DEA Schedule: |
|
