digoxin

Generic: digoxin

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name digoxin
Generic Name digoxin
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

digoxin .125 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-403
Product ID 51655-403_48fee81d-40f1-bacd-e063-6394a90a1342
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215307
Listing Expiration 2027-12-31
Marketing Start 2023-04-13

Pharmacologic Class

Established (EPC)
cardiac glycoside [epc]
Chemical Structure
cardiac glycosides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655403
Hyphenated Format 51655-403

Supplemental Identifiers

RxCUI
197604
UNII
73K4184T59
NUI
N0000175568 M0003451

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name digoxin (source: ndc)
Generic Name digoxin (source: ndc)
Application Number ANDA215307 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .125 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (51655-403-52)
source: ndc

Packages (1)

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

Ingredients (1)

digoxin (.125 mg/1)

Linked Drug Pages (1)

Digoxin ndc-match (0.9)

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"}