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Pramipexole Dihydrochloride

NDC 16714-922, Pramipexole Dihydrochloride, tablet, extended release, from NorthStar RxLLC.

Product NDC
16714-922
Status
Listed
Labeler
NorthStar RxLLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206156
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16714-922 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAMIPEXOLE DIHYDROCHLORIDE4.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
16714-922-011671409220130 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-922-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/946c8a72-8c48-4925-93d3-7940f4c0fd29

  • NADAC price for package 16714092201

    GET /v1/drugs/nadac/16714092201

Use it

Look up 16714-922 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-922 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-922. 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.