Vancomycin Hydrochloride 70436-0023-82

Package NDC

70436-0023-82

Manufacturer: Slate Run Pharmaceuticals, Llc
Dosage Form: Injection, Powder, Lyophilized, For Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: February 6, 2021
Listing Expires: December 31, 2027
Application: ANDA215821

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Active Ingredients

Ingredient	Strength
Vancomycin Hydrochloride	10 g/1

Drug Class

Glycopeptide Antibacterial [EPC]Glycopeptides [CS]

Selected Package

70436-0023-82Selected

1 VIAL in 1 CARTON (70436-023-82) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL