Package 68071-3763-9

Brand: leflunomide

Generic: leflunomide
NDC Package

Package Facts

Identity

Package NDC 68071-3763-9
Digits Only 6807137639
Product NDC 68071-3763
Description

1 BOTTLE in 1 CARTON (68071-3763-9) / 90 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-01-10
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": "2b5ca657-3fa5-8704-e063-6394a90a9f26", "openfda": {"nui": ["N0000175713"], "upc": ["0368071376395"], "unii": ["G162GK9U4W"], "rxcui": ["205284"], "spl_set_id": ["2b5c98d0-de59-85f6-e063-6394a90ab67a"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68071-3763-9)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "68071-3763-9", "marketing_start_date": "20250110"}], "brand_name": "Leflunomide", "product_id": "68071-3763_2b5ca657-3fa5-8704-e063-6394a90a9f26", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "68071-3763", "generic_name": "Leflunomide", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Leflunomide", "active_ingredients": [{"name": "LEFLUNOMIDE", "strength": "10 mg/1"}], "application_number": "ANDA211863", "marketing_category": "ANDA", "marketing_start_date": "20200831", "listing_expiration_date": "20261231"}