Vancomycin Hydrochloride
- Product NDC
- 70860-104
- 11-digit product format
- 708600104
- Labeler code
- 70860
- Product ID
- 70860-104_24074ab6-7ad2-4f91-9190-d74b5936ea0b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vancomycin hydrochloride
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Athenex Pharmaceutical Division, LLC.
- Application
- ANDA205694
- Marketing category
- ANDA
- Marketing start
- 2017-01-01
- Marketing end
- 0000-00-00
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 500 mg/10mL
- Pharmacologic classes
- Glycopeptide Antibacterial [EPC],Glycopeptides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70860-104-10 | 70860010410 | 10 VIAL in 1 CARTON (70860-104-10) > 10 mL in 1 VIAL (70860-104-41) | 10 vial | 2017-09-15 | 0000-00-00 | No | No | Current |