Linezolid
- Product NDC
- 71335-2565
- 11-digit product format
- 713352565
- Labeler code
- 71335
- Product ID
- 71335-2565_c8913686-e7a0-451f-a345-9a8fd6e167df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Linezolid
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205517
- Marketing category
- ANDA
- Marketing start
- 2015-12-21
- Substance
- LINEZOLID
- Active strength
- 600 mg/1
- Pharmacologic classes
- Oxazolidinone Antibacterial [EPC], Oxazolidinones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| ISQ9I6J12J | LINEZOLID | 165800-03-3 | LINEZOLID |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2565-1 | 71335256501 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-2565-1) | 2025-01-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Linezolid | Bryant Ranch Prepack | 2025-08-26 | HUMAN PRESCRIPTION DRUG LABEL | 3 |