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Ropinirole

NDC 69452-358, Ropinirole, tablet, film coated, from Bionpharma Inc..

Product NDC
69452-358
Status
Listed
Labeler
Bionpharma 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/69452-358 \
  -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
69452-358-2069452035820100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-358-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4e6b070c-50a6-4742-af3c-59b45c45735e

  • NADAC price for package 69452035820

    GET /v1/drugs/nadac/69452035820

Use it

Look up 69452-358 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69452-358 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69452-358. 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.