| NDC Code | 16714-856-01 |
|---|
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (16714-856-01) / 25 mL in 1 VIAL, SINGLE-DOSE |
|---|
| Product NDC | 16714-856 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Doxorubicin Hydrochloride |
|---|
| Non-Proprietary Name | Doxorubicin Hydrochloride |
|---|
| Dosage Form | INJECTABLE, LIPOSOMAL |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20170829 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA208657 |
|---|
| Manufacturer | NorthStar RxLLC |
|---|
| Substance Name | DOXORUBICIN HYDROCHLORIDE |
|---|
| Strength | 2 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Anthracycline Topoisomerase Inhibitor [EPC], Anthracyclines [CS], Topoisomerase Inhibitors [MoA] |
|---|