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Pramipexole dihydrochloride

NDC 33342-031, Pramipexole dihydrochloride, tablet, from Macleods Pharmaceuticals Limited.

Product NDC
33342-031
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202164
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/33342-031 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAMIPEXOLE DIHYDROCHLORIDE.125 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
33342-031-063334200310630 BLISTER PACK in 1 CARTON (33342-031-06) / 1 TABLET in 1 BLISTER PACK
33342-031-103334200311090 TABLET in 1 BOTTLE (33342-031-10)
33342-031-1233342003112100 BLISTER PACK in 1 CARTON (33342-031-12) / 1 TABLET in 1 BLISTER PACK
33342-031-1533342003115500 TABLET in 1 BOTTLE (33342-031-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b8c94917-73a1-44c2-8fd8-07f45054176b

Use it

Look up 33342-031 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-031 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-031. 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.