Package 50090-7537-0

Brand: leflunomide

Generic: leflunomide
NDC Package

Package Facts

Identity

Package NDC 50090-7537-0
Digits Only 5009075370
Product NDC 50090-7537
Product ID 50090-7537_183e1875-7234-42e5-bff7-6408e64f2dfe
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-7537-0)

Marketing

Marketing Status
Marketed Since 2025-04-09
Brand leflunomide
Generic leflunomide
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "183e1875-7234-42e5-bff7-6408e64f2dfe", "openfda": {"nui": ["N0000175713"], "unii": ["G162GK9U4W"], "rxcui": ["205285"], "spl_set_id": ["d6f5c510-9ec2-4e2d-b134-25c35bd23fee"], "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 (50090-7537-0)", "package_ndc": "50090-7537-0", "marketing_start_date": "20250409"}], "brand_name": "leflunomide", "product_id": "50090-7537_183e1875-7234-42e5-bff7-6408e64f2dfe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "50090-7537", "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": "ANDA212308", "marketing_category": "ANDA", "marketing_start_date": "20190426", "listing_expiration_date": "20261231"}