| NDC Code | 0069-3033-20 |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0069-3033-20) / 75 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 0069-3033 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Proprietary Name | Doxorubicin Hydrochloride |
| Non-Proprietary Name | Doxorubicin Hydrochloride |
| Dosage Form | INJECTION, SOLUTION |
| Usage | INTRAVENOUS |
| Start Marketing Date | 19871223 |
| 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] |