| NDC Code | 0069-4033-01 |
|---|
| Package Description | 1 VIAL, MULTI-DOSE in 1 PACKAGE (0069-4033-01) > 75 mL in 1 VIAL, MULTI-DOSE |
|---|
| Product NDC | 0069-4033 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Doxorubicin Hydrochloride |
|---|
| Non-Proprietary Name | Doxorubicin Hydrochloride |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20130305 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA050629 |
|---|
| Manufacturer | Pfizer Laboratories Div Pfizer Inc |
|---|
| Substance Name | DOXORUBICIN HYDROCHLORIDE |
|---|
| Strength | 2 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [CS],Topoisomerase Inhibitors [MoA] |
|---|