Package 72789-410-30

Brand: fenofibrate

Generic: fenofibrate
NDC Package

Package Facts

Identity

Package NDC 72789-410-30
Digits Only 7278941030
Product NDC 72789-410
Description

30 TABLET in 1 BOTTLE, PLASTIC (72789-410-30)

Marketing

Marketing Status
Marketed Since 2024-06-05
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": "324713a3-9b23-55ea-e063-6394a90abaab", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "upc": ["0372789410302"], "unii": ["U202363UOS"], "rxcui": ["349287"], "spl_set_id": ["35ba17d9-0dd7-4f15-8f74-be5fd15f1917"], "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": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-410-30)", "package_ndc": "72789-410-30", "marketing_start_date": "20240605"}], "brand_name": "FENOFIBRATE", "product_id": "72789-410_324713a3-9b23-55ea-e063-6394a90abaab", "dosage_form": "TABLET", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "72789-410", "generic_name": "FENOFIBRATE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FENOFIBRATE", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "160 mg/1"}], "application_number": "ANDA076509", "marketing_category": "ANDA", "marketing_start_date": "20220622", "listing_expiration_date": "20261231"}