Vancomycin Hydrochloride
- Product NDC
- 68001-466
- 11-digit product format
- 680010466
- Labeler code
- 68001
- Product ID
- 68001-466_e9578b64-a477-8510-e053-2a95a90a3677
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vancomycin hydrochloride
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- BluePoint Laboratories
- Application
- ANDA204107
- Marketing category
- ANDA
- Marketing start
- 2020-11-30
- Marketing end
- 0000-00-00
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 1 g/1
- Pharmacologic classes
- Glycopeptide Antibacterial [EPC], Glycopeptides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-466-64 | 68001046664 | 10 VIAL, GLASS in 1 CARTON (68001-466-64) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (68001-466-63) | 2020-11-30 | 0000-00-00 | No | No | Current |