Package 72603-134-02

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 72603-134-02
Digits Only 7260313402
Product NDC 72603-134
Product ID 72603-134_04da3e98-02e5-4d5a-94b2-9a6f74c44f15
Description

500 TABLET in 1 BOTTLE (72603-134-02)

Marketing

Marketing Status
Marketed Since 2019-12-13
Brand spironolactone
Generic spironolactone
Sample Package No

Linked Drug Pages (1)

SPIRONOLACTONE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "04da3e98-02e5-4d5a-94b2-9a6f74c44f15", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222", "198223", "313096"], "spl_set_id": ["ae0dcb4e-63df-459c-8e60-0caa817b8135"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-134-01)", "package_ndc": "72603-134-01", "marketing_start_date": "20191213"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72603-134-02)", "package_ndc": "72603-134-02", "marketing_start_date": "20191213"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72603-134-03)", "package_ndc": "72603-134-03", "marketing_start_date": "20191213"}], "brand_name": "SPIRONOLACTONE", "product_id": "72603-134_04da3e98-02e5-4d5a-94b2-9a6f74c44f15", "dosage_form": "TABLET", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "72603-134", "generic_name": "SPIRONOLACTONE", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SPIRONOLACTONE", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA202187", "marketing_category": "ANDA", "marketing_start_date": "20191213", "listing_expiration_date": "20271231"}