Vancomycin Hydrochloride
- Product NDC
- 0409-1319
- 11-digit product format
- 004091319
- Labeler code
- 0409
- Product ID
- 0409-1319_39396834-5ba8-43a0-8ba2-719755e332b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VANCOMYCIN HYDROCHLORIDE
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- ANDA063076
- Marketing category
- ANDA
- Marketing start
- 2021-11-02
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 500 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 0409-1319-01 | 00409131901 | 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0409-1319-01) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE | 2021-11-02 | No | No | Historical |