Package 70518-3118-2

Brand: SPIRONOLACTONE

Generic: SPIRONOLACTONE
NDC Package

Package Facts

Identity

Package NDC 70518-3118-2
Digits Only 7051831182
Product NDC 70518-3118
Product ID 70518-3118_3a1f895d-f849-446e-e063-6394a90a098d
Description

100 TABLET in 1 BOTTLE, PLASTIC (70518-3118-2)

Marketing

Marketing Status
Marketed Since 2023-08-30
Brand SPIRONOLACTONE
Generic SPIRONOLACTONE
Sample Package No

Linked Drug Pages (1)

SPIRONOLACTONE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a1f895d-f849-446e-e063-6394a90a098d", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["313096"], "spl_set_id": ["093f2eb9-7c3b-4960-98cc-30d3d90aa094"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-3118-2)", "package_ndc": "70518-3118-2", "marketing_start_date": "20230830"}], "brand_name": "SPIRONOLACTONE", "product_id": "70518-3118_3a1f895d-f849-446e-e063-6394a90a098d", "dosage_form": "TABLET", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "70518-3118", "generic_name": "SPIRONOLACTONE", "labeler_name": "REMEDYREPACK INC.", "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": "20210610", "listing_expiration_date": "20261231"}