Package 42291-421-30

Brand: leflunomide

Generic: leflunomide
NDC Package

Package Facts

Identity

Package NDC 42291-421-30
Digits Only 4229142130
Product NDC 42291-421
Description

30 TABLET in 1 BOTTLE (42291-421-30)

Marketing

Marketing Status
Marketed Since 2019-06-13
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": "485d0171-db0d-424e-e063-6294a90abcc4", "openfda": {"nui": ["N0000175713"], "unii": ["G162GK9U4W"], "rxcui": ["205284", "205285"], "spl_set_id": ["8b365514-c859-ff93-e053-2a95a90ac698"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (42291-421-30)", "package_ndc": "42291-421-30", "marketing_start_date": "20190613"}], "brand_name": "LEFLUNOMIDE", "product_id": "42291-421_485d0171-db0d-424e-e063-6294a90abcc4", "dosage_form": "TABLET", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "42291-421", "generic_name": "LEFLUNOMIDE", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEFLUNOMIDE", "active_ingredients": [{"name": "LEFLUNOMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077090", "marketing_category": "ANDA", "marketing_start_date": "20190613", "listing_expiration_date": "20271231"}