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Pramipexole Dihydrochloride

NDC 46708-004, Pramipexole Dihydrochloride, tablet, from Alembic Pharmaceuticals Limited.

Product NDC
46708-004
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078894
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-004 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAMIPEXOLE DIHYDROCHLORIDE.25 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
46708-004-904670800049090 TABLET in 1 BOTTLE (46708-004-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/92f6ef1e-3256-45a7-a409-80dd85e95187

Use it

Look up 46708-004 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-004 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-004. 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.