Package 68788-8452-9

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 68788-8452-9
Digits Only 6878884529
Product NDC 68788-8452
Description

90 TABLET, COATED in 1 BOTTLE (68788-8452-9)

Marketing

Marketing Status
Marketed Since 2023-05-30
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": "54a64ac4-2d50-427f-a306-a2e705015502", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198223"], "spl_set_id": ["5e456f3c-f93e-41c6-80c5-a737ed70feda"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (68788-8452-3)", "package_ndc": "68788-8452-3", "marketing_start_date": "20230530"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68788-8452-6)", "package_ndc": "68788-8452-6", "marketing_start_date": "20230530"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (68788-8452-9)", "package_ndc": "68788-8452-9", "marketing_start_date": "20230530"}], "brand_name": "Spironolactone", "product_id": "68788-8452_54a64ac4-2d50-427f-a306-a2e705015502", "dosage_form": "TABLET, COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "68788-8452", "generic_name": "Spironolactone", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "50 mg/1"}], "application_number": "ANDA040750", "marketing_category": "ANDA", "marketing_start_date": "20230530", "listing_expiration_date": "20261231"}