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pramipexole dihydrochloride

NDC 29300-210, pramipexole dihydrochloride, tablet, from Unichem Pharmaceuticals (USA), Inc..

Product NDC
29300-210
Status
Listed
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207011
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/29300-210 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAMIPEXOLE DIHYDROCHLORIDE1 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
29300-210-10293000210101000 TABLET in 1 BOTTLE, PLASTIC (29300-210-10)
29300-210-192930002101990 TABLET in 1 BOTTLE, PLASTIC (29300-210-19)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b978aa75-c62d-444b-9ec6-6c0d21a66688

Use it

Look up 29300-210 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/29300-210 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 29300-210. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.