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Pramipexole Dihydrochloride

NDC 50228-127, Pramipexole Dihydrochloride, tablet, from ScieGen Pharmaceuticals Inc.

Product NDC
50228-127
Status
Listed
Labeler
ScieGen Pharmaceuticals Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203855
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50228-127 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAMIPEXOLE DIHYDROCHLORIDE.25 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
50228-127-10502280127101000 TABLET in 1 BOTTLE (50228-127-10)
50228-127-905022801279090 TABLET in 1 BOTTLE (50228-127-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/395fee34-43dc-4840-a6b8-70d5736f9c8b

  • NADAC price for package 50228012710

    GET /v1/drugs/nadac/50228012710

Use it

Look up 50228-127 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50228-127 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50228-127. 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.