Package 76420-062-60
Brand: spironolactone
Generic: spironolactonePackage Facts
Identity
Package NDC
76420-062-60
Digits Only
7642006260
Product NDC
76420-062
Description
60 TABLET, FILM COATED in 1 BOTTLE (76420-062-60)
Marketing
Marketing Status
Brand
spironolactone
Generic
spironolactone
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "06c94882-1323-c834-e063-6394a90a2d75", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198223", "313096"], "spl_set_id": ["31c42b3e-f076-49d9-aa61-6cef0dbb5543"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76420-062-01)", "package_ndc": "76420-062-01", "marketing_start_date": "20231003"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-062-30)", "package_ndc": "76420-062-30", "marketing_start_date": "20200211"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-062-60)", "package_ndc": "76420-062-60", "marketing_start_date": "20231003"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-062-90)", "package_ndc": "76420-062-90", "marketing_start_date": "20231003"}], "brand_name": "Spironolactone", "product_id": "76420-062_06c94882-1323-c834-e063-6394a90a2d75", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "76420-062", "generic_name": "spironolactone", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA203512", "marketing_category": "ANDA", "marketing_start_date": "20170602", "listing_expiration_date": "20261231"}