Package 71335-2256-2
Brand: leflunomide
Generic: leflunomidePackage Facts
Identity
Package NDC
71335-2256-2
Digits Only
7133522562
Product NDC
71335-2256
Description
90 TABLET, FILM COATED in 1 BOTTLE (71335-2256-2)
Marketing
Marketing Status
Brand
leflunomide
Generic
leflunomide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b94989ef-8c6d-403e-8748-df5bbb5c26eb", "openfda": {"nui": ["N0000175713"], "unii": ["G162GK9U4W"], "rxcui": ["205285"], "spl_set_id": ["acf3efe4-0d70-4718-9c50-789d69ab215d"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2256-1)", "package_ndc": "71335-2256-1", "marketing_start_date": "20230925"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2256-2)", "package_ndc": "71335-2256-2", "marketing_start_date": "20240906"}], "brand_name": "Leflunomide", "product_id": "71335-2256_b94989ef-8c6d-403e-8748-df5bbb5c26eb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "71335-2256", "generic_name": "Leflunomide", "labeler_name": "Bryant Ranch Prepack", "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"}