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Digoxin

NDC 59651-437, Digoxin, tablet, from Aurobindo Pharma Limited.

Product NDC
59651-437
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214982
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-437 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIGOXIN.125 mg/1

Pharmacologic classes

Cardiac Glycoside [EPC]; Cardiac Glycosides [CS]

Package NDCNDC-11Package
59651-437-0159651043701100 TABLET in 1 BOTTLE (59651-437-01)
59651-437-99596510437991000 TABLET in 1 BOTTLE (59651-437-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2bcd56ee-4497-4b8d-84db-a1470c77827b

  • NADAC price for package 59651043701

    GET /v1/drugs/nadac/59651043701

  • NADAC price for package 59651043799

    GET /v1/drugs/nadac/59651043799

Use it

Look up 59651-437 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-437 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-437. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.