Package 35573-448-30

Brand: leflunomide

Generic: leflunomide
NDC Package

Package Facts

Identity

Package NDC 35573-448-30
Digits Only 3557344830
Product NDC 35573-448
Product ID 35573-448_81914a50-0e77-480d-aec5-2889b31a66d3
Description

30 TABLET, FILM COATED in 1 BOTTLE (35573-448-30)

Marketing

Marketing Status
Marketed Since 2022-01-03
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": "81914a50-0e77-480d-aec5-2889b31a66d3", "openfda": {"nui": ["N0000175713"], "unii": ["G162GK9U4W"], "rxcui": ["205284", "205285"], "spl_set_id": ["fc044417-cd9a-42f6-8a3d-a14e7c2f81a2"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Burel Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (35573-448-30)", "package_ndc": "35573-448-30", "marketing_start_date": "20220103"}], "brand_name": "Leflunomide", "product_id": "35573-448_81914a50-0e77-480d-aec5-2889b31a66d3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "35573-448", "generic_name": "leflunomide", "labeler_name": "Burel Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Leflunomide", "active_ingredients": [{"name": "LEFLUNOMIDE", "strength": "20 mg/1"}], "application_number": "ANDA213497", "marketing_category": "ANDA", "marketing_start_date": "20220103", "listing_expiration_date": "20261231"}