Package 63629-1065-1

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 63629-1065-1
Digits Only 6362910651
Product NDC 63629-1065
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-1065-1)

Marketing

Marketing Status
Marketed Since 1986-07-23
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": "118cb0e2-f490-403b-aa8a-0dfbd5ca1c3a", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198223"], "spl_set_id": ["caf41e17-0461-4667-9eab-62853b945131"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-1065-1)", "package_ndc": "63629-1065-1", "marketing_start_date": "19860723"}], "brand_name": "SPIRONOLACTONE", "product_id": "63629-1065_118cb0e2-f490-403b-aa8a-0dfbd5ca1c3a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "63629-1065", "generic_name": "SPIRONOLACTONE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SPIRONOLACTONE", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "50 mg/1"}], "application_number": "ANDA089424", "marketing_category": "ANDA", "marketing_start_date": "19860723", "listing_expiration_date": "20261231"}