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ropinirole

NDC 16729-234, ropinirole, tablet, film coated, from Accord Healthcare Inc..

Product NDC
16729-234
Status
Listed
Labeler
Accord Healthcare Inc.
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/16729-234 \
  -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
16729-234-0116729023401100 TABLET, FILM COATED in 1 BOTTLE (16729-234-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4a2a5b63-5b14-6975-e054-00144ff8d46c

Use it

Look up 16729-234 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16729-234 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16729-234. 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.