NDC 71288-024

Vancomycin hydrochloride 750 mg per 15 mL injection, powder, lyophilized, for solution

On the label: Meitheal Pharmaceuticals Inc..

Where it's made

Kindos Pharmaceuticals Co., Ltd.

Chengdu, China · makes it

Problems found, fixed voluntarily Last FDA inspection Jul 19, 2024. 6 inspections on record.

Product details

Generic drug

Vancomycin: see every company that makes it

Form

injection, powder, lyophilized, for solution, intravenous

Strength

750 mg per 15 mL

Approval

ANDA ANDA215195

On the market since

Sep 15, 2022

Package NDCs

71288-024-20 71288-024-21

Official label

DailyMed (National Library of Medicine), updated Mar 27, 2023

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