Bendamustine Hydrochloride 55150-0392

Product NDC

55150-0392

Manufacturer: Eugia Us Llc
Dosage Form: Injection, Powder, Lyophilized, For Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: June 5, 2023
Listing Expires: December 31, 2026
Application: ANDA214739

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Active Ingredients

Ingredient	Strength
Bendamustine Hydrochloride	100 mg/20mL

Drug Class

Alkylating Activity [MoA]Alkylating Drug [EPC]

Packaging Options(1)

55150-0392-01

1 VIAL, SINGLE-DOSE in 1 CARTON (55150-392-01) / 20 mL in 1 VIAL, SINGLE-DOSE

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