Package 82804-205-30
Brand: spironolactone
Generic: spironolactonePackage Facts
Identity
Package NDC
82804-205-30
Digits Only
8280420530
Product NDC
82804-205
Description
30 TABLET, COATED in 1 BOTTLE (82804-205-30)
Marketing
Marketing Status
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": "34b19a23-4595-417e-9592-fd1d69398e59", "openfda": {"nui": ["N0000175557", "N0000011310"], "upc": ["0382804205301"], "unii": ["27O7W4T232"], "rxcui": ["198222"], "spl_set_id": ["34b19a23-4595-417e-9592-fd1d69398e59"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (82804-205-30)", "package_ndc": "82804-205-30", "marketing_start_date": "20250312"}], "brand_name": "Spironolactone", "product_id": "82804-205_34b19a23-4595-417e-9592-fd1d69398e59", "dosage_form": "TABLET, COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "82804-205", "generic_name": "Spironolactone", "labeler_name": "Proficient Rx LP", "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": "20210104", "listing_expiration_date": "20261231"}