USFDA APPLICATION NUMBER - 50718 / DOSAGE - INJECTABLE, LIPOSOMAL;INJECTION - 50MG/25ML (2MG/ML)
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
doxorubicin hydrochloride(UNII: 82F2G7BL4E) (doxorubicin - UNII:80168379AG) | doxorubicin hydrochloride | 2mg in 1 |
Inactive Ingredients
Ingredient Name | BluePoint Laboratories | Janssen Products, LP |
---|---|---|
AMMONIUM SULFATE(SU46BAM238) | ||
CHOLESTEROL(97C5T2UQ7J) | ||
histidine(4QD397987E) | ||
hydrochloric acid(QTT17582CB) | ||
HYDROGENATED SOYBEAN LECITHIN(H1109Z9J4N) | ||
SODIUM HYDROXIDE(55X04QC32I) | ||
SODIUM N-(CARBONYL-METHOXYPOLYETHYLENE GLYCOL 2000)-1,2-DISTEAROYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE(3L6NN8ZZKU) | ||
SUCROSE(C151H8M554) |
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