Vancomycin Hydrochloride 00338-3582
Product NDC
00338-3582- Manufacturer
- Baxter Healthcare Corporation
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- November 14, 1958
- Listing Expires
- December 31, 2027
- Application
- NDA050671
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Vancomycin Hydrochloride | 750 mg/150mL |
Drug Class
Glycopeptide Antibacterial [EPC]Glycopeptides [CS]
Packaging Options(1)
150 mL in 1 BAG (0338-3582-01)