Package 63629-8539-1

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 63629-8539-1
Digits Only 6362985391
Product NDC 63629-8539
Description

1000 TABLET in 1 BOTTLE, PLASTIC (63629-8539-1)

Marketing

Marketing Status
Marketed Since 1996-07-23
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": "e730d821-976f-4dc5-a98a-4fa3c9539565", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["313096"], "spl_set_id": ["753bbc6f-2e50-49c1-b5bf-18f8411a1e8e"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (63629-8539-1)", "package_ndc": "63629-8539-1", "marketing_start_date": "19960723"}], "brand_name": "SPIRONOLACTONE", "product_id": "63629-8539_e730d821-976f-4dc5-a98a-4fa3c9539565", "dosage_form": "TABLET", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "63629-8539", "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": "ANDA089424", "marketing_category": "ANDA", "marketing_start_date": "19860723", "listing_expiration_date": "20261231"}