NDC 70436-020
Vancomycin Hydrochloride 500 mg injection, powder, lyophilized, for solution
On the label: Slate Run Pharmaceuticals, LLC..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hainan Poly Pharm. Co., Ltd. | Haikou, China | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2023 · 4 inspections |
Product details
- Generic drug
- Vancomycin: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 500 mg
- Approval
- ANDA ANDA212332
- On the market since
- Jun 3, 2019
- Package NDCs
70436-020-82- Official label
- DailyMed (National Library of Medicine), updated May 15, 2026
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