digoxin

Generic: digoxin

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name digoxin
Generic Name digoxin
Labeler avpak
Dosage Form TABLET
Routes
ORAL
Active Ingredients

digoxin .125 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-238
Product ID 50268-238_1cfd158a-1cec-9e3d-e063-6394a90afe49
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214982
Listing Expiration 2026-12-31
Marketing Start 2024-07-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50268238
Hyphenated Format 50268-238

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 ANDA214982 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .125 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 BOX (50268-238-15) / 1 TABLET in 1 BLISTER PACK (50268-238-11)
source: ndc

Packages (1)

50268-238-15 50 BLISTER PACK in 1 BOX (50268-238-15) / 1 TABLET in 1 BLISTER PACK (50268-238-11)

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": "1cfd158a-1cec-9e3d-e063-6394a90afe49", "openfda": {"nui": ["N0000175568", "M0003451"], "unii": ["73K4184T59"], "rxcui": ["197604"], "spl_set_id": ["1cfd4e43-56f0-d182-e063-6394a90ad231"], "pharm_class_cs": ["Cardiac Glycosides [CS]"], "pharm_class_epc": ["Cardiac Glycoside [EPC]"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-238-15)  / 1 TABLET in 1 BLISTER PACK (50268-238-11)", "package_ndc": "50268-238-15", "marketing_start_date": "20240711"}], "brand_name": "Digoxin", "product_id": "50268-238_1cfd158a-1cec-9e3d-e063-6394a90afe49", "dosage_form": "TABLET", "pharm_class": ["Cardiac Glycoside [EPC]", "Cardiac Glycosides [CS]"], "product_ndc": "50268-238", "generic_name": "Digoxin", "labeler_name": "AvPAK", "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": "20240711", "listing_expiration_date": "20261231"}