Package 53746-514-10

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 53746-514-10
Digits Only 5374651410
Product NDC 53746-514
Description

1000 TABLET in 1 BOTTLE (53746-514-10)

Marketing

Marketing Status
Marketed Since 2010-08-02
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": "0b757d66-e1f0-4d56-bbe0-2f0941f0a35e", "openfda": {"nui": ["N0000175557", "N0000011310"], "upc": ["0353746514301", "0353746511300", "0353746515308"], "unii": ["27O7W4T232"], "rxcui": ["198222", "198223", "313096"], "spl_set_id": ["951b8948-dc0f-4aef-9910-82c252de936d"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (53746-514-01)", "package_ndc": "53746-514-01", "marketing_start_date": "20100802"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (53746-514-05)", "package_ndc": "53746-514-05", "marketing_start_date": "20100802"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (53746-514-10)", "package_ndc": "53746-514-10", "marketing_start_date": "20100802"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (53746-514-30)", "package_ndc": "53746-514-30", "marketing_start_date": "20100802"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (53746-514-60)", "package_ndc": "53746-514-60", "marketing_start_date": "20100802"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (53746-514-90)", "package_ndc": "53746-514-90", "marketing_start_date": "20100802"}], "brand_name": "Spironolactone", "product_id": "53746-514_0b757d66-e1f0-4d56-bbe0-2f0941f0a35e", "dosage_form": "TABLET", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "53746-514", "generic_name": "Spironolactone", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "50 mg/1"}], "application_number": "ANDA091426", "marketing_category": "ANDA", "marketing_start_date": "20100802", "listing_expiration_date": "20261231"}