Linezolid
- Product NDC
- 0093-7490
- 11-digit product format
- 000937490
- Labeler code
- 0093
- Product ID
- 0093-7490_e3e2ef09-2e46-48c0-90e8-bb5bcba67cba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Linezolid
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA078061
- Marketing category
- ANDA
- Marketing start
- 2016-06-03
- Marketing end
- 2020-05-31
- Substance
- LINEZOLID
- Active strength
- 600 mg/1
- Pharmacologic classes
- Oxazolidinone Antibacterial [EPC],Oxazolidinones [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record