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NDC 71770-105, hydroxyurea, tablet, film coated, from Medunik.

Product NDC
71770-105
Status
Listed
Labeler
Medunik
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA208843
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71770-105 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROXYUREA100 mg/1

Pharmacologic classes

Antimetabolite [EPC]; Urea [CS]

Package NDCNDC-11Package
71770-105-60717700105601 BOTTLE in 1 CARTON (71770-105-60) / 60 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/76957c0d-0f98-4376-bb06-eee651adc09d
  • NADAC price for package 71770010560

    GET /v1/drugs/nadac/71770010560

Use it

Look up 71770-105 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71770-105 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71770-105. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.