Package 71335-0741-1

Brand: fenofibrate

Generic: fenofibrate
NDC Package

Package Facts

Identity

Package NDC 71335-0741-1
Digits Only 7133507411
Product NDC 71335-0741
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-0741-1)

Marketing

Marketing Status
Marketed Since 2018-03-16
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": "01c33ccd-f3ff-40c4-901e-fecc9b1c7791", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "unii": ["U202363UOS"], "rxcui": ["349287"], "spl_set_id": ["40ca5d88-6403-4c4b-ae7f-ae8cec4d9965"], "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": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0741-1)", "package_ndc": "71335-0741-1", "marketing_start_date": "20180316"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0741-2)", "package_ndc": "71335-0741-2", "marketing_start_date": "20180316"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0741-3)", "package_ndc": "71335-0741-3", "marketing_start_date": "20211227"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (71335-0741-4)", "package_ndc": "71335-0741-4", "marketing_start_date": "20211227"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-0741-5)", "package_ndc": "71335-0741-5", "marketing_start_date": "20211227"}], "brand_name": "Fenofibrate", "product_id": "71335-0741_01c33ccd-f3ff-40c4-901e-fecc9b1c7791", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "71335-0741", "generic_name": "Fenofibrate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "160 mg/1"}], "application_number": "ANDA076433", "marketing_category": "ANDA", "marketing_start_date": "20170601", "listing_expiration_date": "20261231"}