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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Linezolid
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LINEZOLID | 600 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ISQ9I6J12J |
| Rxcui | 311347 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2565-1 | Linezolid | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-2565 | LINEZOLID TABLET, FILM COATED [BRYANT RANCH PREPACK] | 1 | Current NDC, 1 package rows | 20250130_ab1b4ab5-7338-4b01-963b-43eeb4c9cf1c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |