Package 71335-2887-1
Brand: spironolactone
Generic: spironolactonePackage Facts
Identity
Package NDC
71335-2887-1
Digits Only
7133528871
Product NDC
71335-2887
Description
100 TABLET, FILM COATED in 1 BOTTLE (71335-2887-1)
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": "587353ec-0515-4398-83cd-14abc4f49ae9", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198223"], "spl_set_id": ["be4aa233-1555-4972-858e-46343a710558"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-2887-1)", "package_ndc": "71335-2887-1", "marketing_start_date": "20251028"}], "brand_name": "SPIRONOLACTONE", "product_id": "71335-2887_587353ec-0515-4398-83cd-14abc4f49ae9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "71335-2887", "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": "ANDA089424", "marketing_category": "ANDA", "marketing_start_date": "19860723", "listing_expiration_date": "20261231"}