Package 72189-496-30
Brand: spironolactone
Generic: spironolactonePackage Facts
Identity
Package NDC
72189-496-30
Digits Only
7218949630
Product NDC
72189-496
Description
30 TABLET, COATED in 1 BOTTLE (72189-496-30)
Marketing
Marketing Status
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": "2c4e3f99-d912-b742-e063-6294a90a5d1d", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198223"], "spl_set_id": ["ffd1ed7a-b6a4-4240-e053-6394a90a7db1"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (72189-496-30)", "package_ndc": "72189-496-30", "marketing_start_date": "20230706"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (72189-496-90)", "package_ndc": "72189-496-90", "marketing_start_date": "20230706"}], "brand_name": "Spironolactone", "product_id": "72189-496_2c4e3f99-d912-b742-e063-6294a90a5d1d", "dosage_form": "TABLET, COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "72189-496", "generic_name": "Spironolactone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "50 mg/1"}], "application_number": "ANDA040750", "marketing_category": "ANDA", "marketing_start_date": "20230706", "listing_expiration_date": "20261231"}