Leflunomide
- Product NDC
- 72266-133
- 11-digit product format
- 722660133
- Labeler code
- 72266
- Product ID
- 72266-133_ed9cae73-77b4-4811-e053-2995a90a8511
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Leflunomide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Fosun Pharma USA Inc.
- Application
- ANDA077087
- Marketing category
- ANDA
- Marketing start
- 2022-11-16
- Marketing end
- 0000-00-00
- Substance
- LEFLUNOMIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Antirheumatic Agent [EPC]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72266-133-50 | 72266013350 | 30 TABLET in 1 BOTTLE (72266-133-50) | 30 tablet | 2022-11-16 | 0000-00-00 | No | No | Current |