Doxorubicin Hydrochloride 47335-0049
Product NDC
47335-0049- 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]
Packaging Options(1)
1 VIAL, SINGLE-DOSE in 1 PACKAGE (47335-049-40) / 10 mL in 1 VIAL, SINGLE-DOSE