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Pramipexole Dihydrochloride

NDC 57237-180, Pramipexole Dihydrochloride, tablet, from Rising Pharma Holdings, Inc..

Product NDC
57237-180
Status
Listed
Labeler
Rising Pharma Holdings, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202633
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57237-180 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAMIPEXOLE DIHYDROCHLORIDE.125 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
57237-180-905723701809090 TABLET in 1 BOTTLE (57237-180-90)
57237-180-99572370180991000 TABLET in 1 BOTTLE (57237-180-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/56e8d1f6-6dbf-4e11-a177-a56bbfb9f8ec

  • NADAC price for package 57237018090

    GET /v1/drugs/nadac/57237018090

Use it

Look up 57237-180 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57237-180 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57237-180. 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.