Doxorubicin Hydrochloride 68001-0629
Product NDC
68001-0629- Manufacturer
- Bluepoint Laboratories
- Dosage Form
- Injection, Suspension, Liposomal
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- January 7, 2025
- 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(2)
1 VIAL, SINGLE-USE in 1 CARTON (68001-629-26) / 25 mL in 1 VIAL, SINGLE-USE
1 VIAL, SINGLE-USE in 1 CARTON (68001-629-36) / 10 mL in 1 VIAL, SINGLE-USE