vancomycin hydrochloride
- Product NDC
- 67457-612
- 11-digit product format
- 674570612
- Labeler code
- 67457
- Product ID
- 67457-612_62f3a37d-1748-4f97-8d32-a1dd3c5ed869
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vancomycin hydrochloride
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Mylan Institutional LLC
- Application
- ANDA065397
- Marketing category
- ANDA
- Marketing start
- 2008-12-31
- Marketing end
- 0000-00-00
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 1 g/20mL
- Pharmacologic classes
- Glycopeptide Antibacterial [EPC],Glycopeptides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67457-612-20 | 67457061220 | 10 VIAL in 1 CARTON (67457-612-20) > 20 mL in 1 VIAL | 10 vial | 2008-12-31 | 0000-00-00 | No | No | Current |