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DOXIL
DOXIL - 59676-960-01 - (doxorubicin hydrochloride)
Drug Information of DOXIL
| Product NDC: | 59676-960 |
| Proprietary Name: | DOXIL |
| Non Proprietary Name: | doxorubicin hydrochloride |
| Active Ingredient(s): | 2 mg/mL & nbsp; doxorubicin hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SUSPENSION, LIPOSOMAL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DOXIL
| Product NDC: | 59676-960 |
| Labeler Name: | Janssen Products, LP |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050718 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19951117 |
Package Information of DOXIL
| Package NDC: | 59676-960-01 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (59676-960-01) > 10 mL in 1 VIAL, SINGLE-USE |
NDC Information of DOXIL
| NDC Code | 59676-960-01 |
| Proprietary Name | DOXIL |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (59676-960-01) > 10 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 59676-960 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | doxorubicin hydrochloride |
| Dosage Form Name | INJECTION, SUSPENSION, LIPOSOMAL |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19951117 |
| Marketing Category Name | NDA |
| Labeler Name | Janssen Products, LP |
| Substance Name | DOXORUBICIN HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
