Package 70748-130-06

Brand: leflunomide

Generic: leflunomide
NDC Package

Package Facts

Identity

Package NDC 70748-130-06
Digits Only 7074813006
Product NDC 70748-130
Description

30 TABLET, FILM COATED in 1 BOTTLE (70748-130-06)

Marketing

Marketing Status
Marketed Since 2020-08-31
Brand leflunomide
Generic leflunomide
Sample Package No

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5d28a5cf-ca54-4fcc-a459-2be6ba1afb3e", "openfda": {"nui": ["N0000175713"], "upc": ["0370748129067", "0370748130063"], "unii": ["G162GK9U4W"], "rxcui": ["205284", "205285"], "spl_set_id": ["5d48fded-b43b-461a-8488-ca1da5c41a03"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70748-130-06)", "package_ndc": "70748-130-06", "marketing_start_date": "20200831"}], "brand_name": "Leflunomide", "product_id": "70748-130_5d28a5cf-ca54-4fcc-a459-2be6ba1afb3e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "70748-130", "generic_name": "Leflunomide", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Leflunomide", "active_ingredients": [{"name": "LEFLUNOMIDE", "strength": "20 mg/1"}], "application_number": "ANDA211863", "marketing_category": "ANDA", "marketing_start_date": "20200831", "listing_expiration_date": "20261231"}