leflunomide
Generic: leflunomide
Labeler: burel pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
leflunomide
Generic Name
leflunomide
Labeler
burel pharmaceuticals, llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
leflunomide 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
35573-448
Product ID
35573-448_81914a50-0e77-480d-aec5-2889b31a66d3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213497
Listing Expiration
2026-12-31
Marketing Start
2022-01-03
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
35573448
Hyphenated Format
35573-448
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
leflunomide (source: ndc)
Generic Name
leflunomide (source: ndc)
Application Number
ANDA213497 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (35573-448-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "81914a50-0e77-480d-aec5-2889b31a66d3", "openfda": {"nui": ["N0000175713"], "unii": ["G162GK9U4W"], "rxcui": ["205284", "205285"], "spl_set_id": ["fc044417-cd9a-42f6-8a3d-a14e7c2f81a2"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Burel Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (35573-448-30)", "package_ndc": "35573-448-30", "marketing_start_date": "20220103"}], "brand_name": "Leflunomide", "product_id": "35573-448_81914a50-0e77-480d-aec5-2889b31a66d3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "35573-448", "generic_name": "leflunomide", "labeler_name": "Burel Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Leflunomide", "active_ingredients": [{"name": "LEFLUNOMIDE", "strength": "20 mg/1"}], "application_number": "ANDA213497", "marketing_category": "ANDA", "marketing_start_date": "20220103", "listing_expiration_date": "20261231"}