Package 59651-349-30

Brand: leflunomide

Generic: leflunomide
NDC Package

Package Facts

Identity

Package NDC 59651-349-30
Digits Only 5965134930
Product NDC 59651-349
Product ID 59651-349_e4a1828b-43bf-42dd-af71-5f9a3d49023c
Description

30 TABLET, FILM COATED in 1 BOTTLE (59651-349-30)

Marketing

Marketing Status
Marketed Since 2021-03-29
Brand leflunomide
Generic leflunomide
Sample Package No

Linked Drug Pages (1)

Leflunomide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e4a1828b-43bf-42dd-af71-5f9a3d49023c", "openfda": {"nui": ["N0000175713"], "unii": ["G162GK9U4W"], "rxcui": ["205284", "205285"], "spl_set_id": ["c358276a-610e-46da-b81a-95c837af205d"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (59651-349-30)", "package_ndc": "59651-349-30", "marketing_start_date": "20210329"}], "brand_name": "Leflunomide", "product_id": "59651-349_e4a1828b-43bf-42dd-af71-5f9a3d49023c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "59651-349", "generic_name": "Leflunomide", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Leflunomide", "active_ingredients": [{"name": "LEFLUNOMIDE", "strength": "20 mg/1"}], "application_number": "ANDA213652", "marketing_category": "ANDA", "marketing_start_date": "20210329", "listing_expiration_date": "20261231"}