Package 73352-101-01

Brand: fenofibrate

Generic: fenofibrate
NDC Package

Package Facts

Identity

Package NDC 73352-101-01
Digits Only 7335210101
Product NDC 73352-101
Description

90 TABLET in 1 BOTTLE (73352-101-01)

Marketing

Marketing Status
Marketed Since 2025-08-12
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": "3c3539f7-7a1e-8fd3-e063-6294a90a1082", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "upc": ["0373352101016", "0373352102013"], "unii": ["U202363UOS"], "rxcui": ["749802", "749804"], "spl_set_id": ["3c3539e4-bc4a-8152-e063-6294a90ab55c"], "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": ["Trifluent Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (73352-101-01)", "package_ndc": "73352-101-01", "marketing_start_date": "20250812"}], "brand_name": "FENOFIBRATE", "product_id": "73352-101_3c3539f7-7a1e-8fd3-e063-6294a90a1082", "dosage_form": "TABLET", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "73352-101", "generic_name": "fenofibrate", "labeler_name": "Trifluent Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FENOFIBRATE", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "40 mg/1"}], "application_number": "ANDA217732", "marketing_category": "ANDA", "marketing_start_date": "20250812", "listing_expiration_date": "20261231"}