Linezolid
- Product NDC
- 68382-413
- 11-digit product format
- 683820413
- Labeler code
- 68382
- Product ID
- 68382-413_936ad52c-acf7-45da-9c28-7cf85e61fcdb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Linezolid
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA206097
- Marketing category
- ANDA
- Marketing start
- 2017-08-09
- Marketing end
- 0000-00-00
- Substance
- LINEZOLID
- Active strength
- 600 mg/1
- Pharmacologic classes
- Oxazolidinone Antibacterial [EPC], Oxazolidinones [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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68382-413-01 | 68382041301 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-413-01) | 2017-08-09 | 0000-00-00 | No | No | Current |
| 68382-413-05 | 68382041305 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-413-05) | 2017-08-09 | 0000-00-00 | No | No | Current |
| 68382-413-06 | 68382041306 | 30 TABLET, FILM COATED in 1 BOTTLE (68382-413-06) | 2017-08-09 | 0000-00-00 | No | No | Current |
| 68382-413-10 | 68382041310 | 1000 TABLET, FILM COATED in 1 BOTTLE (68382-413-10) | 2017-08-09 | 0000-00-00 | No | No | Current |
| 68382-413-16 | 68382041316 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-413-16) | 2017-08-09 | 0000-00-00 | No | No | Current |
| 68382-413-92 | 68382041392 | 20 TABLET, FILM COATED in 1 BOTTLE (68382-413-92) | 2017-08-09 | 0000-00-00 | No | No | Current |