Package 16729-227-01

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 16729-227-01
Digits Only 1672922701
Product NDC 16729-227
Description

100 TABLET, FILM COATED in 1 BOTTLE (16729-227-01)

Marketing

Marketing Status
Marketed Since 2017-06-02
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": "44e7bdd1-ae77-4b63-e063-6294a90a2c28", "openfda": {"nui": ["N0000175557", "N0000011310"], "upc": ["0316729227018", "0316729225014", "0316729226011"], "unii": ["27O7W4T232"], "rxcui": ["198222", "198223", "313096"], "spl_set_id": ["8a96e2c9-049a-43ab-abf3-21baedeb736f"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Accord Healthcare, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16729-227-01)", "package_ndc": "16729-227-01", "marketing_start_date": "20170602"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (16729-227-16)", "package_ndc": "16729-227-16", "marketing_start_date": "20170602"}], "brand_name": "Spironolactone", "product_id": "16729-227_44e7bdd1-ae77-4b63-e063-6294a90a2c28", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "16729-227", "generic_name": "spironolactone", "labeler_name": "Accord Healthcare, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "100 mg/1"}], "application_number": "ANDA203512", "marketing_category": "ANDA", "marketing_start_date": "20170602", "listing_expiration_date": "20261231"}