Vancomycin Hydrochloride 70594-0122
Product NDC
70594-0122- Manufacturer
- Xellia Pharmaceuticals Usa Llc
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- February 23, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA205694
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Vancomycin Hydrochloride | 500 mg/1 |
Drug Class
Glycopeptide Antibacterial [EPC]Glycopeptides [CS]
Packaging Options(1)
10 VIAL, GLASS in 1 CARTON (70594-122-02) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS (70594-122-01)