digoxin
Generic: digoxin
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
digoxin
Generic Name
digoxin
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
digoxin 250 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6588
Product ID
50090-6588_82287cb4-5de6-4470-ae7d-fa65e8b30c3a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076363
Listing Expiration
2026-12-31
Marketing Start
2016-09-12
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906588
Hyphenated Format
50090-6588
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA076363 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 ug/1
Packaging
- 100 TABLET in 1 BOTTLE (50090-6588-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "82287cb4-5de6-4470-ae7d-fa65e8b30c3a", "openfda": {"nui": ["N0000175568", "M0003451"], "unii": ["73K4184T59"], "rxcui": ["197606"], "spl_set_id": ["0a88434e-4a1b-4ade-a51e-38145e22a232"], "pharm_class_cs": ["Cardiac Glycosides [CS]"], "pharm_class_epc": ["Cardiac Glycoside [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-6588-1)", "package_ndc": "50090-6588-1", "marketing_start_date": "20230810"}], "brand_name": "Digoxin", "product_id": "50090-6588_82287cb4-5de6-4470-ae7d-fa65e8b30c3a", "dosage_form": "TABLET", "pharm_class": ["Cardiac Glycoside [EPC]", "Cardiac Glycosides [CS]"], "product_ndc": "50090-6588", "generic_name": "Digoxin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digoxin", "active_ingredients": [{"name": "DIGOXIN", "strength": "250 ug/1"}], "application_number": "ANDA076363", "marketing_category": "ANDA", "marketing_start_date": "20160912", "listing_expiration_date": "20261231"}