Dalbavancin 71839-0144

Product NDC

71839-0144

Manufacturer: Be Pharmaceuticals Inc.
Dosage Form: Injection, Powder, Lyophilized, For Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: June 12, 2026
Listing Expires: December 31, 2027
Application: ANDA219604

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Active Ingredients

Ingredient	Strength
Dalbavancin Hydrochloride	500 mg/25mL

Drug Class

Lipoglycopeptide Antibacterial [EPC]Lipoglycopeptides [CS]

Packaging Options(1)

71839-0144-01

1 VIAL in 1 CARTON (71839-144-01) / 25 mL in 1 VIAL

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