Package 71335-2204-1

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 71335-2204-1
Digits Only 7133522041
Product NDC 71335-2204
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2204-1)

Marketing

Marketing Status
Marketed Since 2023-08-04
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": "9bf28452-222f-407a-95da-a534d27fed3e", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222"], "spl_set_id": ["1c31c953-05ce-475a-b93f-80aeb12bde95"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2204-1)", "package_ndc": "71335-2204-1", "marketing_start_date": "20230804"}], "brand_name": "SPIRONOLACTONE", "product_id": "71335-2204_9bf28452-222f-407a-95da-a534d27fed3e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "71335-2204", "generic_name": "SPIRONOLACTONE", "labeler_name": "Bryant Ranch Prepack", "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"}