Package 50090-5992-0

Brand: leflunomide

Generic: leflunomide
NDC Package

Package 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
Marketed Since 2022-06-10
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"}