Package 71335-0401-4
Brand: spironolactone
Generic: spironolactonePackage Facts
Identity
Package NDC
71335-0401-4
Digits Only
7133504014
Product NDC
71335-0401
Description
100 TABLET, FILM COATED in 1 BOTTLE (71335-0401-4)
Marketing
Marketing Status
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": "473dc80f-11b7-46bf-b0b4-7a271444fca2", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198223"], "spl_set_id": ["473dc80f-11b7-46bf-b0b4-7a271444fca2"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0401-1)", "package_ndc": "71335-0401-1", "marketing_start_date": "20220209"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0401-2)", "package_ndc": "71335-0401-2", "marketing_start_date": "20220209"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0401-3)", "package_ndc": "71335-0401-3", "marketing_start_date": "20220209"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-0401-4)", "package_ndc": "71335-0401-4", "marketing_start_date": "20220209"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (71335-0401-5)", "package_ndc": "71335-0401-5", "marketing_start_date": "20220209"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-0401-6)", "package_ndc": "71335-0401-6", "marketing_start_date": "20220209"}], "brand_name": "Spironolactone", "product_id": "71335-0401_473dc80f-11b7-46bf-b0b4-7a271444fca2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "71335-0401", "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": "ANDA203512", "marketing_category": "ANDA", "marketing_start_date": "20170602", "listing_expiration_date": "20261231"}