Package 50090-5992-0
Brand: leflunomide
Generic: leflunomidePackage Facts
Identity
Package NDC
50090-5992-0
Digits Only
5009059920
Product NDC
50090-5992
Description
30 TABLET, FILM COATED in 1 BOTTLE (50090-5992-0)
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": "81afc9f2-c82b-4373-80fb-f8c00942c79a", "openfda": {"nui": ["N0000175713"], "unii": ["G162GK9U4W"], "rxcui": ["205285"], "spl_set_id": ["0a4f8671-b632-4cc5-8dc9-6b863e62b467"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-5992-0)", "package_ndc": "50090-5992-0", "marketing_start_date": "20220610"}], "brand_name": "Leflunomide", "product_id": "50090-5992_81afc9f2-c82b-4373-80fb-f8c00942c79a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "50090-5992", "generic_name": "Leflunomide", "labeler_name": "A-S Medication Solutions", "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"}