Package 62332-554-90

Brand: fenofibrate

Generic: fenofibrate
NDC Package

Package Facts

Identity

Package NDC 62332-554-90
Digits Only 6233255490
Product NDC 62332-554
Description

90 TABLET, FILM COATED in 1 BOTTLE (62332-554-90)

Marketing

Marketing Status
Marketed Since 2019-08-01
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": "ffa16afa-35e9-4845-a0e4-f8b290bd5da4", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "unii": ["U202363UOS"], "rxcui": ["349287", "351133"], "spl_set_id": ["2985c70d-e85d-483e-8d36-7a4b8454b038"], "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": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62332-554-90)", "package_ndc": "62332-554-90", "marketing_start_date": "20190801"}], "brand_name": "Fenofibrate", "product_id": "62332-554_ffa16afa-35e9-4845-a0e4-f8b290bd5da4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "62332-554", "generic_name": "Fenofibrate", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "54 mg/1"}], "application_number": "ANDA209660", "marketing_category": "ANDA", "marketing_start_date": "20190801", "listing_expiration_date": "20261231"}