VANCOMYCIN HYDROCHLORIDE
- Product NDC
- 0338-0122
- 11-digit product format
- 003380122
- Labeler code
- 0338
- Product ID
- 0338-0122_4e548f07-0e95-4ae7-bda2-176cb4a781fd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VANCOMYCIN HYDROCHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVITREAL
- Labeler
- Baxter Healthcare Corporation
- Application
- NDA050671
- Marketing category
- NDA
- Marketing start
- 1958-11-14
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 1.25 g/250mL
- Pharmacologic classes
- Glycopeptide Antibacterial [EPC], Glycopeptides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 0338-0122-04 | 00338012204 | 250 mL in 1 BAG (0338-0122-04) | 250 ml | 2024-01-25 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| VANCOMYCIN HYDROCHLORIDE | Baxter Healthcare Corporation | 2025-03-13 | HUMAN PRESCRIPTION DRUG LABEL | 26 |