Package 72189-495-90

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 72189-495-90
Digits Only 7218949590
Product NDC 72189-495
Description

90 TABLET, COATED in 1 BOTTLE (72189-495-90)

Marketing

Marketing Status
Marketed Since 2023-07-05
Brand spironolactone
Generic spironolactone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4e3760-8448-4adb-e063-6394a90a5ffc", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222"], "spl_set_id": ["ffc2e9b4-1f0f-220c-e053-6294a90a6d75"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (72189-495-90)", "package_ndc": "72189-495-90", "marketing_start_date": "20230705"}], "brand_name": "Spironolactone", "product_id": "72189-495_2c4e3760-8448-4adb-e063-6394a90a5ffc", "dosage_form": "TABLET, COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "72189-495", "generic_name": "Spironolactone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "100 mg/1"}], "application_number": "ANDA040750", "marketing_category": "ANDA", "marketing_start_date": "20230705", "listing_expiration_date": "20261231"}