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pramipexole dihydrochloride

NDC 64380-747, pramipexole dihydrochloride, tablet, from Strides Pharma Science Limited.

Product NDC
64380-747
Status
Listed
Labeler
Strides Pharma Science Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202702
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/64380-747 \
  -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
64380-747-016438007470110 BLISTER PACK in 1 CARTON (64380-747-01) / 10 TABLET in 1 BLISTER PACK
64380-747-056438007470590 TABLET in 1 BOTTLE (64380-747-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fb2260d6-204c-4d25-a331-0f8340d83a6e

  • NADAC price for package 64380074705

    GET /v1/drugs/nadac/64380074705

Use it

Look up 64380-747 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/64380-747 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 64380-747. 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.