| NDC Code | 0069-0171-01 |
|---|
| Package Description | 25 mL in 1 VIAL (0069-0171-01) |
|---|
| Product NDC | 0069-0171 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Doxorubicin Hydrochloride |
|---|
| Non-Proprietary Name | Doxorubicin Hydrochloride |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20111029 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA200170 |
|---|
| Manufacturer | Pfizer Laboratories Div Pfizer Inc. |
|---|
| Substance Name | DOXORUBICIN HYDROCHLORIDE |
|---|
| Strength | 2 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
|---|