Package 71335-2205-1
Brand: spironolactone
Generic: spironolactonePackage Facts
Identity
Package NDC
71335-2205-1
Digits Only
7133522051
Product NDC
71335-2205
Description
500 TABLET in 1 BOTTLE, PLASTIC (71335-2205-1)
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": "8c23f39e-6044-41e9-bd14-df509e70967c", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["313096"], "spl_set_id": ["2d0655d7-fda6-40c6-907c-acaba0e19987"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (71335-2205-1)", "package_ndc": "71335-2205-1", "marketing_start_date": "20230804"}], "brand_name": "SPIRONOLACTONE", "product_id": "71335-2205_8c23f39e-6044-41e9-bd14-df509e70967c", "dosage_form": "TABLET", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "71335-2205", "generic_name": "SPIRONOLACTONE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SPIRONOLACTONE", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA089424", "marketing_category": "ANDA", "marketing_start_date": "19860723", "listing_expiration_date": "20261231"}