Package 0025-1041-31

Brand: aldactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 0025-1041-31
Digits Only 0025104131
Product NDC 0025-1041
Description

100 TABLET, FILM COATED in 1 BOTTLE (0025-1041-31)

Marketing

Marketing Status
Marketed Since 1960-01-21
Brand aldactone
Generic spironolactone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "22946678-dcad-4518-9bc6-cbdf51a38c16", "openfda": {"nui": ["N0000175557", "N0000011310"], "upc": ["0300251001314", "0300251031311", "0300251041310"], "unii": ["27O7W4T232"], "rxcui": ["198222", "198223", "200817", "200820", "200825", "313096"], "spl_set_id": ["0fed2822-3a03-4b64-9857-c682fcd462bc"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0025-1041-31)", "package_ndc": "0025-1041-31", "marketing_start_date": "19600121"}], "brand_name": "Aldactone", "product_id": "0025-1041_22946678-dcad-4518-9bc6-cbdf51a38c16", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "0025-1041", "generic_name": "spironolactone", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aldactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "50 mg/1"}], "application_number": "NDA012151", "marketing_category": "NDA", "marketing_start_date": "19600121", "listing_expiration_date": "20261231"}