Doxorubicin Hydrochloride 70748-0340
Product NDC
70748-0340- Manufacturer
- Lupin Pharmaceuticals, Inc.
- Dosage Form
- Injection, Suspension, Liposomal
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- August 26, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA215178
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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-USE in 1 CARTON (70748-340-01) / 25 mL in 1 VIAL, SINGLE-USE