NDC 70436-021

Vancomycin Hydrochloride 1 g injection, powder, lyophilized, for solution

On the label: Slate Run Pharmaceuticals, LLC..

Where it's made

Hainan Poly Pharm. Co., Ltd.

Haikou, China · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Jun 30, 2023. 4 inspections on record.

Product details

Generic drug
Vancomycin: see every company that makes it
Form
injection, powder, lyophilized, for solution, intravenous
Strength
1 g
Approval
ANDA ANDA212332
On the market since
Jun 3, 2019
Package NDCs
70436-021-82
Official label
DailyMed (National Library of Medicine), updated May 15, 2026

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