Package 68071-3764-9

Brand: leflunomide

Generic: leflunomide
NDC Package

Package Facts

Identity

Package NDC 68071-3764-9
Digits Only 6807137649
Product NDC 68071-3764
Product ID 68071-3764_2b5f2b4f-bea9-b661-e063-6294a90ad251
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-3764-9)

Marketing

Marketing Status
Marketed Since 2025-01-09
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": "2b5f2b4f-bea9-b661-e063-6294a90ad251", "openfda": {"nui": ["N0000175713"], "upc": ["0368071376494"], "unii": ["G162GK9U4W"], "rxcui": ["205285"], "spl_set_id": ["2b5f387e-b52b-ad80-e063-6394a90a56d5"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-3764-9)", "package_ndc": "68071-3764-9", "marketing_start_date": "20250109"}], "brand_name": "leflunomide", "product_id": "68071-3764_2b5f2b4f-bea9-b661-e063-6294a90ad251", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "68071-3764", "generic_name": "leflunomide", "labeler_name": "NuCare Pharmaceuticals, Inc.", "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"}