Vancomycin Hydrochloride
- Product NDC
- 71335-2948
- 11-digit product format
- 713352948
- Labeler code
- 71335
- Product ID
- 71335-2948_bbbbe78c-d261-4630-8abb-b653a6f9a479
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vancomycin Hydrochloride
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA061667
- Marketing category
- ANDA
- Marketing start
- 2019-09-09
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 250 mg/5mL
- Pharmacologic classes
- Glycopeptide Antibacterial [EPC], Glycopeptides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 71WO621TJD | VANCOMYCIN HYDROCHLORIDE | 1404-93-9 | VANCOMYCIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2948-1 | 71335294801 | 80 mL in 1 BOTTLE (71335-2948-1) | 80 ml | 2025-11-06 | No | No | Historical |