Package 72162-2409-3

Brand: leflunomide

Generic: leflunomide
NDC Package

Package Facts

Identity

Package NDC 72162-2409-3
Digits Only 7216224093
Product NDC 72162-2409
Product ID 72162-2409_8cc23541-0457-4fc2-8098-4cdf8f5a0d1a
Description

30 TABLET in 1 BOTTLE (72162-2409-3)

Marketing

Marketing Status
Marketed Since 2024-10-30
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": "8cc23541-0457-4fc2-8098-4cdf8f5a0d1a", "openfda": {"nui": ["N0000175713"], "unii": ["G162GK9U4W"], "rxcui": ["205284"], "spl_set_id": ["e76d7767-744f-4e52-956d-e59f7a924826"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2409-3)", "package_ndc": "72162-2409-3", "marketing_start_date": "20241030"}], "brand_name": "leflunomide", "product_id": "72162-2409_8cc23541-0457-4fc2-8098-4cdf8f5a0d1a", "dosage_form": "TABLET", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "72162-2409", "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"}