Package 70771-1492-1

Brand: leflunomide

Generic: leflunomide
NDC Package

Package Facts

Identity

Package NDC 70771-1492-1
Digits Only 7077114921
Product NDC 70771-1492
Description

100 TABLET, FILM COATED in 1 BOTTLE (70771-1492-1)

Marketing

Marketing Status
Marketed Since 2019-04-26
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": "e96c4125-a2bf-420c-8ffe-6d7ddb7dd645", "openfda": {"nui": ["N0000175713"], "unii": ["G162GK9U4W"], "rxcui": ["205284", "205285"], "spl_set_id": ["c66cacd1-93f7-483a-a2fc-aad53d5342b0"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70771-1492-1)", "package_ndc": "70771-1492-1", "marketing_start_date": "20190426"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70771-1492-3)", "package_ndc": "70771-1492-3", "marketing_start_date": "20190426"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70771-1492-5)", "package_ndc": "70771-1492-5", "marketing_start_date": "20190426"}], "brand_name": "leflunomide", "product_id": "70771-1492_e96c4125-a2bf-420c-8ffe-6d7ddb7dd645", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "70771-1492", "generic_name": "leflunomide", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "leflunomide", "active_ingredients": [{"name": "LEFLUNOMIDE", "strength": "20 mg/1"}], "application_number": "ANDA212308", "marketing_category": "ANDA", "marketing_start_date": "20190426", "listing_expiration_date": "20261231"}