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Pramipexole Dihydrochloride

NDC 33342-213, Pramipexole Dihydrochloride, tablet, extended release, from Macleods Pharmaceuticals Limited.

Product NDC
33342-213
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
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/33342-213 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAMIPEXOLE DIHYDROCHLORIDE3.75 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
33342-213-073334202130730 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-213-07)
33342-213-123334202131210 BLISTER PACK in 1 CARTON (33342-213-12) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1dbb8d2f-e0d9-4f8b-89d2-2a03496ef7be

Use it

Look up 33342-213 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-213 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-213. 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.