Package 71335-2874-1

Brand: leflunomide

Generic: leflunomide
NDC Package

Package Facts

Identity

Package NDC 71335-2874-1
Digits Only 7133528741
Product NDC 71335-2874
Product ID 71335-2874_c09fb831-4b93-47e8-9c95-2082c73ce4c6
Description

30 TABLET in 1 BOTTLE (71335-2874-1)

Marketing

Marketing Status
Marketed Since 2025-10-22
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": "c09fb831-4b93-47e8-9c95-2082c73ce4c6", "openfda": {"nui": ["N0000175713"], "unii": ["G162GK9U4W"], "rxcui": ["205284"], "spl_set_id": ["d0fb9685-9e54-44e5-b543-1077e1a620c6"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2874-1)", "package_ndc": "71335-2874-1", "marketing_start_date": "20251022"}], "brand_name": "leflunomide", "product_id": "71335-2874_c09fb831-4b93-47e8-9c95-2082c73ce4c6", "dosage_form": "TABLET", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "71335-2874", "generic_name": "leflunomide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "leflunomide", "active_ingredients": [{"name": "LEFLUNOMIDE", "strength": "10 mg/1"}], "application_number": "ANDA077086", "marketing_category": "ANDA", "marketing_start_date": "20091029", "listing_expiration_date": "20261231"}