Package 68071-3795-9

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 68071-3795-9
Digits Only 6807137959
Product NDC 68071-3795
Description

90 TABLET in 1 BOTTLE (68071-3795-9)

Marketing

Marketing Status
Marketed Since 2025-02-17
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": "2e5e782d-9cec-d4a4-e063-6294a90aba3a", "openfda": {"nui": ["N0000175557", "N0000011310"], "upc": ["0368071379594"], "unii": ["27O7W4T232"], "rxcui": ["198223"], "spl_set_id": ["2e5e782d-9ceb-d4a4-e063-6294a90aba3a"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3795-9)", "package_ndc": "68071-3795-9", "marketing_start_date": "20250217"}], "brand_name": "SPIRONOLACTONE", "product_id": "68071-3795_2e5e782d-9cec-d4a4-e063-6294a90aba3a", "dosage_form": "TABLET", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "68071-3795", "generic_name": "SPIRONOLACTONE", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SPIRONOLACTONE", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "50 mg/1"}], "application_number": "ANDA202187", "marketing_category": "ANDA", "marketing_start_date": "20191213", "listing_expiration_date": "20261231"}