Package 63187-861-30

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 63187-861-30
Digits Only 6318786130
Product NDC 63187-861
Description

30 TABLET, FILM COATED in 1 BOTTLE (63187-861-30)

Marketing

Marketing Status
Marketed Since 2017-06-01
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": "d5bfc979-a820-4d06-ab41-9ccbaf28a914", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198223"], "spl_set_id": ["caf9c845-63eb-40bd-8261-0582abdf705a"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-861-30)", "package_ndc": "63187-861-30", "marketing_start_date": "20170601"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-861-60)", "package_ndc": "63187-861-60", "marketing_start_date": "20170601"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-861-90)", "package_ndc": "63187-861-90", "marketing_start_date": "20170601"}], "brand_name": "Spironolactone", "product_id": "63187-861_d5bfc979-a820-4d06-ab41-9ccbaf28a914", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "63187-861", "generic_name": "spironolactone", "labeler_name": "Proficient Rx LP", "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"}