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Desmopressin Acetate

NDC 10702-169, Desmopressin Acetate, tablet, from KVK-TECH, INC..

Product NDC
10702-169
Status
Listed
Labeler
KVK-TECH, INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210371
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10702-169 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DESMOPRESSIN ACETATE.1 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
10702-169-0110702016901100 TABLET in 1 BOTTLE (10702-169-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9fba5e90-f541-4588-a5e9-b56198f17e87

Use it

Look up 10702-169 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10702-169 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10702-169. 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.