Package 51655-344-26

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 51655-344-26
Digits Only 5165534426
Product NDC 51655-344
Description

90 TABLET, FILM COATED in 1 BOTTLE (51655-344-26)

Marketing

Marketing Status
Marketed Since 2020-05-27
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": "48eb2ef1-10f5-aa75-e063-6294a90a901f", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222"], "spl_set_id": ["ab3090fc-458c-17c1-e053-2995a90a6ffa"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (51655-344-26)", "package_ndc": "51655-344-26", "marketing_start_date": "20200527"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-344-52)", "package_ndc": "51655-344-52", "marketing_start_date": "20200824"}], "brand_name": "Spironolactone", "product_id": "51655-344_48eb2ef1-10f5-aa75-e063-6294a90a901f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "51655-344", "generic_name": "spironolactone", "labeler_name": "Northwind Health Company, LLC", "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": "20200527", "listing_expiration_date": "20271231"}