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Pramipexole Dihydrochloride Extended-Release

NDC 69680-145, Pramipexole Dihydrochloride, tablet, extended release, from Vitruvias Therapeutics, Inc..

Product NDC
69680-145
Status
Listed
Labeler
Vitruvias Therapeutics, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212797
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69680-145 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAMIPEXOLE DIHYDROCHLORIDE.375 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
69680-145-306968001453030 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-145-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d07aad1b-e078-4fca-8386-ca2e8e899688

  • NADAC price for package 69680014530

    GET /v1/drugs/nadac/69680014530

Use it

Look up 69680-145 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69680-145 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69680-145. 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.