Package 42708-101-30

Brand: spironolactone

Generic: spironolactone
NDC Package Sample

Package Facts

Identity

Package NDC 42708-101-30
Digits Only 4270810130
Product NDC 42708-101
Description

30 TABLET, FILM COATED in 1 BOTTLE (42708-101-30)

Marketing

Marketing Status
Marketed Since 2019-10-18
Brand spironolactone
Generic spironolactone
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "458698e8-b92c-e278-e063-6394a90a1a05", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["313096"], "spl_set_id": ["37066684-5b63-4d3e-ae6a-08c4b3edd7aa"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42708-101-30)", "package_ndc": "42708-101-30", "marketing_start_date": "20191018"}], "brand_name": "Spironolactone", "product_id": "42708-101_458698e8-b92c-e278-e063-6394a90a1a05", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "42708-101", "generic_name": "spironolactone", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA203253", "marketing_category": "ANDA", "marketing_start_date": "20130201", "listing_expiration_date": "20261231"}