Package 16714-590-02

Brand: digoxin

Generic: digoxin
NDC Package

Package Facts

Identity

Package NDC 16714-590-02
Digits Only 1671459002
Product NDC 16714-590
Description

1000 TABLET in 1 BOTTLE (16714-590-02)

Marketing

Marketing Status
Discontinued 2026-04-30
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": "9e663767-1f4a-4a9b-9571-fe7ba0ff10f5", "openfda": {"nui": ["N0000175568", "M0003451"], "unii": ["73K4184T59"], "rxcui": ["197604", "197606"], "spl_set_id": ["8ec4abe0-7974-4921-b542-c9673dc5f77f"], "pharm_class_cs": ["Cardiac Glycosides [CS]"], "pharm_class_epc": ["Cardiac Glycoside [EPC]"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (16714-590-02)", "package_ndc": "16714-590-02", "marketing_end_date": "20260430", "marketing_start_date": "20160912"}], "brand_name": "Digoxin", "product_id": "16714-590_9e663767-1f4a-4a9b-9571-fe7ba0ff10f5", "dosage_form": "TABLET", "pharm_class": ["Cardiac Glycoside [EPC]", "Cardiac Glycosides [CS]"], "product_ndc": "16714-590", "generic_name": "Digoxin", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digoxin", "active_ingredients": [{"name": "DIGOXIN", "strength": "125 ug/1"}], "application_number": "ANDA076363", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20160912"}