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Pramipexole Dihydrochloride

NDC 46708-580, Pramipexole Dihydrochloride, tablet, extended release, from Alembic Pharmaceuticals Limited.

Product NDC
46708-580
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204518
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-580 \
  -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
46708-580-304670805803030 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-580-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b6935240-ee81-49ef-adad-fb900d7f5127

Use it

Look up 46708-580 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-580 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-580. 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.