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ropinirole hydrochloride

NDC 43547-597, ropinirole hydrochloride, tablet, film coated, from SOLCO HEALTHCARE US, LLC.

Product NDC
43547-597
Status
Listed
Labeler
SOLCO HEALTHCARE US, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078110
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43547-597 \
  -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
43547-597-1043547059710100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-597-10)
43547-597-5043547059750500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-597-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5823b3a2-3256-4d94-97b4-ec6b940312f4

Use it

Look up 43547-597 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43547-597 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43547-597. 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.