Package 68788-8381-6

Brand: spironolactone

Generic: spironolactone
NDC Package

Package Facts

Identity

Package NDC 68788-8381-6
Digits Only 6878883816
Product NDC 68788-8381
Description

60 TABLET, COATED in 1 BOTTLE (68788-8381-6)

Marketing

Marketing Status
Marketed Since 2023-02-28
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": "fa4ec5d1-d864-40f3-bdd0-47ff9d87586d", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222"], "spl_set_id": ["b68235bb-0940-4810-bbf4-2a7a0881de68"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (68788-8381-3)", "package_ndc": "68788-8381-3", "marketing_start_date": "20230228"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68788-8381-6)", "package_ndc": "68788-8381-6", "marketing_start_date": "20230228"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (68788-8381-9)", "package_ndc": "68788-8381-9", "marketing_start_date": "20230228"}], "brand_name": "Spironolactone", "product_id": "68788-8381_fa4ec5d1-d864-40f3-bdd0-47ff9d87586d", "dosage_form": "TABLET, COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "68788-8381", "generic_name": "Spironolactone", "labeler_name": "Preferred Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "100 mg/1"}], "application_number": "ANDA040750", "marketing_category": "ANDA", "marketing_start_date": "20230228", "listing_expiration_date": "20261231"}