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Desmopressin Acetate

NDC 59651-250, desmopressin acetate, tablet, from Aurobindo Pharma Limited.

Product NDC
59651-250
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213095
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-250 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DESMOPRESSIN ACETATE.2 mg/1

Pharmacologic classes

Factor VIII Activator [EPC]; Increased Coagulation Factor VIII Activity [PE]; Increased Coagulation Factor VIII Concentration [PE]; Vasopressin Analog [EPC]; Vasopressins [CS]

Package NDCNDC-11Package
59651-250-0159651025001100 TABLET in 1 BOTTLE (59651-250-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/24866ad0-94db-46a2-96c0-b362acd0271a

  • NADAC price for package 59651025001

    GET /v1/drugs/nadac/59651025001

Use it

Look up 59651-250 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-250 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-250. 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.