Package 72162-2150-5
Brand: spironolactone
Generic: spironolactonePackage Facts
Identity
Package NDC
72162-2150-5
Digits Only
7216221505
Product NDC
72162-2150
Description
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2150-5)
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": "221eb6a5-7e95-4219-9d19-9415d4578a38", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["313096"], "spl_set_id": ["ce792c44-421d-4274-a333-01e2297ee0a3"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2150-5)", "package_ndc": "72162-2150-5", "marketing_start_date": "20231207"}], "brand_name": "Spironolactone", "product_id": "72162-2150_221eb6a5-7e95-4219-9d19-9415d4578a38", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "72162-2150", "generic_name": "spironolactone", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA040424", "marketing_category": "ANDA", "marketing_start_date": "19810203", "listing_expiration_date": "20261231"}