Package 68382-660-16
Brand: spironolactone
Generic: spironolactonePackage Facts
Identity
Package NDC
68382-660-16
Digits Only
6838266016
Product NDC
68382-660
Description
90 TABLET, FILM COATED in 1 BOTTLE (68382-660-16)
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": "79b8df9c-5a73-432e-bd16-bbbecd9e2046", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222", "198223", "313096"], "spl_set_id": ["99bbc053-0e41-4b4d-979a-db610908f2de"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68382-660-01)", "package_ndc": "68382-660-01", "marketing_start_date": "20180815"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68382-660-05)", "package_ndc": "68382-660-05", "marketing_start_date": "20180815"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68382-660-06)", "package_ndc": "68382-660-06", "marketing_start_date": "20180815"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68382-660-10)", "package_ndc": "68382-660-10", "marketing_start_date": "20180815"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68382-660-16)", "package_ndc": "68382-660-16", "marketing_start_date": "20180815"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68382-660-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "68382-660-30", "marketing_start_date": "20180815"}], "brand_name": "spironolactone", "product_id": "68382-660_79b8df9c-5a73-432e-bd16-bbbecd9e2046", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "68382-660", "generic_name": "spironolactone", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA205936", "marketing_category": "ANDA", "marketing_start_date": "20180815", "listing_expiration_date": "20261231"}