Vancomycin Hydrochloride
- Product NDC
- 47781-598
- 11-digit product format
- 477810598
- Labeler code
- 47781
- Product ID
- 47781-598_477dcb18-55f4-dc92-fe3b-5fb483fe6c5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vancomycin hydrochloride
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Alvogen Inc.
- Application
- ANDA205694
- Marketing category
- ANDA
- Marketing start
- 2017-08-28
- Marketing end
- 2022-04-01
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 500 mg/10mL
- Pharmacologic classes
- Glycopeptide Antibacterial [EPC],Glycopeptides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 47781-598-91 | 47781059891 | 10 VIAL in 1 CARTON (47781-598-91) > 10 mL in 1 VIAL (47781-598-07) | 10 vial | 2017-08-28 | 2022-04-01 | No | No | Current |