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Pramipexole Dihydrochloride

NDC 65862-605, Pramipexole Dihydrochloride, tablet, from Aurobindo Pharma Limited.

Product NDC
65862-605
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202633
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-605 \
  -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
65862-605-786586206057810 BLISTER PACK in 1 CARTON (65862-605-78) / 10 TABLET in 1 BLISTER PACK (65862-605-10)
65862-605-906586206059090 TABLET in 1 BOTTLE (65862-605-90)
65862-605-99658620605991000 TABLET in 1 BOTTLE (65862-605-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3f90971a-e005-4dd3-bb93-b09125ada3c8

Use it

Look up 65862-605 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-605 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-605. 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.