Package 72162-1694-1

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 72162-1694-1
Digits Only 7216216941
Product NDC 72162-1694
Description

100 TABLET, FILM COATED in 1 BOTTLE (72162-1694-1)

Marketing

Marketing Status
Marketed Since 2017-04-04
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": "818e4d5d-d5cf-46a3-acd9-3609f344cd2e", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198223"], "spl_set_id": ["b5b129b8-aed9-4d94-a35e-e92647effbdb"], "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 (72162-1694-1)", "package_ndc": "72162-1694-1", "marketing_start_date": "20170404"}], "brand_name": "Spironolactone", "product_id": "72162-1694_818e4d5d-d5cf-46a3-acd9-3609f344cd2e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "72162-1694", "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": "ANDA203253", "marketing_category": "ANDA", "marketing_start_date": "20130201", "listing_expiration_date": "20261231"}