Doxorubicin Hydrochloride 47335-0049-40

Package NDC

47335-0049-40

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Injectable, Liposomal
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: February 5, 2013
Listing Expires: December 31, 2027
Application: ANDA203263

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Active Ingredients

Ingredient	Strength
Doxorubicin Hydrochloride	2 mg/mL

Drug Class

Anthracycline Topoisomerase Inhibitor [EPC]Anthracyclines [CS]Topoisomerase Inhibitors [MoA]

Selected Package

47335-0049-40Selected

1 VIAL, SINGLE-DOSE in 1 PACKAGE (47335-049-40) / 10 mL in 1 VIAL, SINGLE-DOSE