Package 63629-1094-1

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 63629-1094-1
Digits Only 6362910941
Product NDC 63629-1094
Description

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-1094-1)

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": "37122f93-9a22-4ae4-b5c8-040cef92f936", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222"], "spl_set_id": ["0cc23419-e6d5-4036-8011-dc1d2455e0cb"], "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 (63629-1094-1)", "package_ndc": "63629-1094-1", "marketing_start_date": "19860723"}], "brand_name": "SPIRONOLACTONE", "product_id": "63629-1094_37122f93-9a22-4ae4-b5c8-040cef92f936", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "63629-1094", "generic_name": "SPIRONOLACTONE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SPIRONOLACTONE", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "100 mg/1"}], "application_number": "ANDA089424", "marketing_category": "ANDA", "marketing_start_date": "19860723", "listing_expiration_date": "20261231"}