Package 67046-1636-3

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 67046-1636-3
Digits Only 6704616363
Product NDC 67046-1636
Description

30 TABLET, COATED in 1 BLISTER PACK (67046-1636-3)

Marketing

Marketing Status
Marketed Since 2025-12-30
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": "472ef1b9-ede4-a39d-e063-6294a90ad566", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222"], "spl_set_id": ["472ee2ad-7e57-bef1-e063-6394a90a0206"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BLISTER PACK (67046-1636-3)", "package_ndc": "67046-1636-3", "marketing_start_date": "20251230"}], "brand_name": "Spironolactone", "product_id": "67046-1636_472ef1b9-ede4-a39d-e063-6294a90ad566", "dosage_form": "TABLET, COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "67046-1636", "generic_name": "Spironolactone", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "100 mg/1"}], "application_number": "ANDA040750", "marketing_category": "ANDA", "marketing_start_date": "20251230", "listing_expiration_date": "20261231"}