Leflunomide
- Product NDC
- 13811-677
- 11-digit product format
- 138110677
- Labeler code
- 13811
- Product ID
- 13811-677_a664123b-9725-4c37-8856-55e2304b9ecf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Leflunomide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Trigen Laboratories, LLC
- Application
- ANDA091369
- Marketing category
- ANDA
- Marketing start
- 2011-05-06
- Marketing end
- 2019-12-31
- Substance
- LEFLUNOMIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Antirheumatic Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record