Package 68071-2369-9

Brand: fenofibrate

Generic: fenofibrate
NDC Package

Package Facts

Identity

Package NDC 68071-2369-9
Digits Only 6807123699
Product NDC 68071-2369
Description

90 TABLET, COATED in 1 BOTTLE (68071-2369-9)

Marketing

Marketing Status
Marketed Since 2021-03-17
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": "4b45622d-5001-33a3-e063-6394a90afb6e", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "upc": ["0368071236996"], "unii": ["U202363UOS"], "rxcui": ["477562"], "spl_set_id": ["bdc2211e-6d65-1500-e053-2a95a90ab145"], "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": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (68071-2369-9)", "package_ndc": "68071-2369-9", "marketing_start_date": "20210317"}], "brand_name": "Fenofibrate", "product_id": "68071-2369_4b45622d-5001-33a3-e063-6394a90afb6e", "dosage_form": "TABLET, COATED", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "68071-2369", "generic_name": "Fenofibrate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "48 mg/1"}], "application_number": "ANDA205118", "marketing_category": "ANDA", "marketing_start_date": "20160505", "listing_expiration_date": "20271231"}