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ROPINIROLE

NDC 72189-222, ROPINIROLE, tablet, film coated, from DIRECT RX.

Product NDC
72189-222
Status
Listed
Labeler
DIRECT RX
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204022
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-222 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ROPINIROLE HYDROCHLORIDE1 mg/1

Pharmacologic classes

Dopamine Agonists [MoA]; Nonergot Dopamine Agonist [EPC]

Package NDCNDC-11Package
72189-222-307218902223030 TABLET, FILM COATED in 1 BOTTLE (72189-222-30)
72189-222-607218902226060 TABLET, FILM COATED in 1 BOTTLE (72189-222-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c2c38b4c-b139-45f2-e053-2995a90a262c

Use it

Look up 72189-222 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-222 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-222. 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.