leflunomide
- Product NDC
- 68071-3764
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- leflunomide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA212308
- Marketing category
- ANDA
- Substance
- LEFLUNOMIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3764-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3764-9) | 2025-01-09 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| leflunomide | NuCare Pharmaceuticals, Inc. | 2025-01-10 | HUMAN PRESCRIPTION DRUG LABEL | 1 |