Package 68180-389-09

Brand: fenofibrate

Generic: fenofibrate
NDC Package

Package Facts

Identity

Package NDC 68180-389-09
Digits Only 6818038909
Product NDC 68180-389
Description

90 TABLET in 1 BOTTLE (68180-389-09)

Marketing

Marketing Status
Marketed Since 2020-08-01
Brand fenofibrate
Generic fenofibrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e454c5bc-7a0e-4d5e-95fb-ccf812747a3c", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "unii": ["U202363UOS"], "rxcui": ["477560", "477562"], "spl_set_id": ["45364845-c3b4-40a1-a677-82202ffaa5ad"], "pharm_class_cs": ["Fibric Acids [CS]"], "pharm_class_epc": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "pharm_class_moa": ["Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (68180-389-02)", "package_ndc": "68180-389-02", "marketing_start_date": "20200801"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68180-389-09)", "package_ndc": "68180-389-09", "marketing_start_date": "20200801"}], "brand_name": "Fenofibrate", "product_id": "68180-389_e454c5bc-7a0e-4d5e-95fb-ccf812747a3c", "dosage_form": "TABLET", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "68180-389", "generic_name": "Fenofibrate", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "145 mg/1"}], "application_number": "ANDA090856", "marketing_category": "ANDA", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}