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Ropinirole

NDC 10135-676, ropinirole, tablet, film coated, from Marlex Pharmaceuticals Inc.

Product NDC
10135-676
Status
Listed
Labeler
Marlex Pharmaceuticals Inc
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA079165
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10135-676 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ROPINIROLE HYDROCHLORIDE2 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
10135-676-0110135067601100 TABLET, FILM COATED in 1 BOTTLE (10135-676-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/35d90f6f-3116-4afa-be2d-b65c160e8ab3

Use it

Look up 10135-676 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10135-676 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10135-676. 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.