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Pramipexole dihydrochloride

NDC 55111-612, Pramipexole dihydrochloride, tablet, extended release, from Dr. Reddy's Laboratories Limited.

Product NDC
55111-612
Status
Listed
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203354
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55111-612 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAMIPEXOLE DIHYDROCHLORIDE.75 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
55111-612-305511106123030 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-612-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/00699692-532a-68fd-8a51-3770a81b2208

  • NADAC price for package 55111061230

    GET /v1/drugs/nadac/55111061230

Use it

Look up 55111-612 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55111-612 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55111-612. 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.