VANCOMYCIN HYDROCHLORIDE
- Product NDC
- 23155-219
- 11-digit product format
- 231550219
- Labeler code
- 23155
- Product ID
- 23155-219_7744ab78-80f5-424b-a6c5-46a957367375
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VANCOMYCIN HYDROCHLORIDE
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Application
- ANDA202274
- Marketing category
- ANDA
- Marketing start
- 2011-11-25
- Marketing end
- 0000-00-00
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 5 g/100mL
- Pharmacologic classes
- Glycopeptide Antibacterial [EPC],Glycopeptides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record