Package 70518-3859-0

Brand: digoxin

Generic: digoxin
NDC Package

Package Facts

Identity

Package NDC 70518-3859-0
Digits Only 7051838590
Product NDC 70518-3859
Description

30 TABLET in 1 BLISTER PACK (70518-3859-0)

Marketing

Marketing Status
Marketed Since 2023-09-11
Brand digoxin
Generic digoxin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f8ca510-9119-898d-e063-6394a90ad212", "openfda": {"nui": ["N0000175568", "M0003451"], "unii": ["73K4184T59"], "rxcui": ["197604"], "spl_set_id": ["dbc0bc24-f250-47e8-8d10-6aef551823d7"], "pharm_class_cs": ["Cardiac Glycosides [CS]"], "pharm_class_epc": ["Cardiac Glycoside [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3859-0)", "package_ndc": "70518-3859-0", "marketing_start_date": "20230911"}], "brand_name": "Digoxin", "product_id": "70518-3859_3f8ca510-9119-898d-e063-6394a90ad212", "dosage_form": "TABLET", "pharm_class": ["Cardiac Glycoside [EPC]", "Cardiac Glycosides [CS]"], "product_ndc": "70518-3859", "generic_name": "Digoxin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digoxin", "active_ingredients": [{"name": "DIGOXIN", "strength": ".125 mg/1"}], "application_number": "ANDA214982", "marketing_category": "ANDA", "marketing_start_date": "20230911", "listing_expiration_date": "20261231"}