Package 53489-328-06

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 53489-328-06
Digits Only 5348932806
Product NDC 53489-328
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-06)

Marketing

Marketing Status
Marketed Since 1986-07-23
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": "d58f76e0-60c3-42ec-8375-128cd42485f1", "openfda": {"nui": ["N0000175557", "N0000011310"], "upc": ["0353489143011", "0353489329019"], "unii": ["27O7W4T232"], "rxcui": ["198222", "198223", "313096"], "spl_set_id": ["c23b6b9b-aec3-48a8-a518-76e4097f6479"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-01)", "package_ndc": "53489-328-01", "marketing_start_date": "19860723"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-02)", "package_ndc": "53489-328-02", "marketing_start_date": "19860723"}, {"sample": false, "description": "250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-03)", "package_ndc": "53489-328-03", "marketing_start_date": "19860723"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-05)", "package_ndc": "53489-328-05", "marketing_start_date": "19860723"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-06)", "package_ndc": "53489-328-06", "marketing_start_date": "19860723"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-07)", "package_ndc": "53489-328-07", "marketing_start_date": "19860723"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-10)", "package_ndc": "53489-328-10", "marketing_start_date": "19860723"}], "brand_name": "SPIRONOLACTONE", "product_id": "53489-328_d58f76e0-60c3-42ec-8375-128cd42485f1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "53489-328", "generic_name": "SPIRONOLACTONE", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SPIRONOLACTONE", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "50 mg/1"}], "application_number": "ANDA089424", "marketing_category": "ANDA", "marketing_start_date": "19860723", "listing_expiration_date": "20261231"}