LENALIDOMIDE
- Product NDC
- 70710-1030
- 11-digit product format
- 707101030
- Labeler code
- 70710
- Product ID
- 70710-1030_d06dec99-06d1-4525-9caf-460747b53fbc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LENALIDOMIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA210154
- Marketing category
- ANDA
- Marketing start
- 2023-03-07
- Substance
- LENALIDOMIDE
- Active strength
- 2.5 mg/1
- Pharmacologic classes
- Thalidomide Analog [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| F0P408N6V4 | LENALIDOMIDE | 191732-72-6 | LENALIDOMIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70710-1030-1 | 70710103001 | 100 CAPSULE in 1 BOTTLE (70710-1030-1) | 100 capsule | 2023-03-07 | No | No | Historical |
| 70710-1030-7 | 70710103007 | 28 CAPSULE in 1 BOTTLE (70710-1030-7) | 28 capsule | 2023-03-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LENALIDOMIDE | Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | 2024-02-10 | HUMAN PRESCRIPTION DRUG LABEL | 7 |