Package 50090-6432-1

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 50090-6432-1
Digits Only 5009064321
Product NDC 50090-6432
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-6432-1)

Marketing

Marketing Status
Marketed Since 2023-04-11
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": "aba7ca7e-edbd-4b42-8491-4b0f6361bab8", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222"], "spl_set_id": ["4514fa40-613e-46f5-bee4-3edc7cc9863f"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6432-0)", "package_ndc": "50090-6432-0", "marketing_start_date": "20230411"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6432-1)", "package_ndc": "50090-6432-1", "marketing_start_date": "20230411"}], "brand_name": "SPIRONOLACTONE", "product_id": "50090-6432_aba7ca7e-edbd-4b42-8491-4b0f6361bab8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "50090-6432", "generic_name": "SPIRONOLACTONE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SPIRONOLACTONE", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "100 mg/1"}], "application_number": "ANDA089424", "marketing_category": "ANDA", "marketing_start_date": "19860723", "listing_expiration_date": "20261231"}