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Ropinirole

NDC 71335-2515, Ropinirole, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-2515
Status
Listed
Labeler
Bryant Ranch Prepack
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/71335-2515 \
  -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
71335-2515-17133525150130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-1)
71335-2515-27133525150260 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-2)
71335-2515-37133525150390 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2515-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/af340f28-92b2-49af-b651-b9b01ca3ce6c

Use it

Look up 71335-2515 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2515 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2515. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.