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Ropinirole

NDC 87063-200, Ropinirole, tablet, film coated, from ASCLEMED USA INC..

Product NDC
87063-200
Status
Listed
Labeler
ASCLEMED USA INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA079229
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/87063-200 \
  -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
87063-200-0187063020001100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-200-01)
87063-200-308706302003030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-200-30)
87063-200-608706302006060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-200-60)
87063-200-908706302009090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-200-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8f3612f0-0976-4de7-a1d6-eabaa8b75f9c

Use it

Look up 87063-200 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87063-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87063-200. 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.