Package 51655-403-52

Brand: digoxin

Generic: digoxin
NDC Package

Package Facts

Identity

Package NDC 51655-403-52
Digits Only 5165540352
Product NDC 51655-403
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-403-52)

Marketing

Marketing Status
Marketed Since 2023-04-13
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": "48fee81d-40f1-bacd-e063-6394a90a1342", "openfda": {"nui": ["N0000175568", "M0003451"], "unii": ["73K4184T59"], "rxcui": ["197604"], "spl_set_id": ["f9897bec-c16f-2728-e053-6394a90aecb7"], "pharm_class_cs": ["Cardiac Glycosides [CS]"], "pharm_class_epc": ["Cardiac Glycoside [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-403-52)", "package_ndc": "51655-403-52", "marketing_start_date": "20230413"}], "brand_name": "Digoxin", "product_id": "51655-403_48fee81d-40f1-bacd-e063-6394a90a1342", "dosage_form": "TABLET", "pharm_class": ["Cardiac Glycoside [EPC]", "Cardiac Glycosides [CS]"], "product_ndc": "51655-403", "generic_name": "Digoxin", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digoxin", "active_ingredients": [{"name": "DIGOXIN", "strength": ".125 mg/1"}], "application_number": "ANDA215307", "marketing_category": "ANDA", "marketing_start_date": "20230413", "listing_expiration_date": "20271231"}