Vancomycin Hydrochloride 70436-0020
Product NDC
70436-0020- Manufacturer
- Slate Run Pharmaceuticals, Llc
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- June 3, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA212332
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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 in 1 CARTON (70436-020-82) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL