Package 0378-0243-05

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 0378-0243-05
Digits Only 0378024305
Product NDC 0378-0243
Description

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0243-05)

Marketing

Marketing Status
Marketed Since 2009-06-26
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": "8df5eab3-b5f9-4c98-8a62-4bd4c905c6b1", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222", "198223", "313096"], "spl_set_id": ["beaf74db-4159-3b59-ef99-575c3ac99aa1"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0243-01)", "package_ndc": "0378-0243-01", "marketing_start_date": "20020122"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0243-05)", "package_ndc": "0378-0243-05", "marketing_start_date": "20090626"}], "brand_name": "Spironolactone", "product_id": "0378-0243_8df5eab3-b5f9-4c98-8a62-4bd4c905c6b1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "0378-0243", "generic_name": "spironolactone", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "50 mg/1"}], "application_number": "ANDA040424", "marketing_category": "ANDA", "marketing_start_date": "20020122", "listing_expiration_date": "20271231"}