Vancomycin Hydrochloride
- Product NDC
- 52584-332
- 11-digit product format
- 525840332
- Labeler code
- 52584
- Product ID
- 52584-332_b7c6c4e5-1714-4595-8705-cd75eb3db4ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vancomycin Hydrochloride
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA062911
- Marketing category
- ANDA
- Marketing start
- 2010-09-01
- Marketing end
- 0000-00-00
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 500 mg/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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-332-01 | 52584033201 | 1 VIAL in 1 BAG (52584-332-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL | 1 vial | 2010-09-01 | 0000-00-00 | No | No | Current |