Package 43598-909-90

Brand: fenofibrate

Generic: fenofibrate
NDC Package

Package Facts

Identity

Package NDC 43598-909-90
Digits Only 4359890990
Product NDC 43598-909
Product ID 43598-909_f1aa7987-8d7b-4df7-81e1-884966cf0173
Description

90 TABLET, FILM COATED in 1 BOTTLE (43598-909-90)

Marketing

Marketing Status
Marketed Since 2020-01-31
Brand fenofibrate
Generic fenofibrate
Sample Package No

Linked Drug Pages (1)

Fenofibrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f1aa7987-8d7b-4df7-81e1-884966cf0173", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "upc": ["0343598910901", "0343598909905"], "unii": ["U202363UOS"], "rxcui": ["349287", "351133"], "spl_set_id": ["9e69d844-5ded-46b6-8321-c420e8b37a63"], "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": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (43598-909-90)", "package_ndc": "43598-909-90", "marketing_start_date": "20200131"}], "brand_name": "Fenofibrate", "product_id": "43598-909_f1aa7987-8d7b-4df7-81e1-884966cf0173", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "43598-909", "generic_name": "FENOFIBRATE", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "54 mg/1"}], "application_number": "ANDA210670", "marketing_category": "ANDA", "marketing_start_date": "20200131", "listing_expiration_date": "20261231"}