Package 71335-2832-1

Brand: leflunomide

Generic: leflunomide
NDC Package

Package Facts

Identity

Package NDC 71335-2832-1
Digits Only 7133528321
Product NDC 71335-2832
Product ID 71335-2832_a057209f-4e79-48e8-a749-60772266b573
Description

30 TABLET in 1 BOTTLE (71335-2832-1)

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": "a057209f-4e79-48e8-a749-60772266b573", "openfda": {"nui": ["N0000175713"], "unii": ["G162GK9U4W"], "rxcui": ["205285"], "spl_set_id": ["fa5f71b3-6a56-4616-baf7-4b761023b2a9"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2832-1)", "package_ndc": "71335-2832-1", "marketing_start_date": "20251022"}], "brand_name": "leflunomide", "product_id": "71335-2832_a057209f-4e79-48e8-a749-60772266b573", "dosage_form": "TABLET", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "71335-2832", "generic_name": "leflunomide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "leflunomide", "active_ingredients": [{"name": "LEFLUNOMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077086", "marketing_category": "ANDA", "marketing_start_date": "20091029", "listing_expiration_date": "20261231"}