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PRAMIPEXOLE

NDC 31722-906, PRAMIPEXOLE, tablet, from Camber Pharmaceuticals, Inc..

Product NDC
31722-906
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203855
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-906 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAMIPEXOLE DIHYDROCHLORIDE.125 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
31722-906-0531722090605500 TABLET in 1 BOTTLE (31722-906-05)
31722-906-10317220906101000 TABLET in 1 BOTTLE (31722-906-10)
31722-906-903172209069090 TABLET in 1 BOTTLE (31722-906-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a7405a56-de1c-4875-b57f-210c991474ba

Use it

Look up 31722-906 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-906 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-906. 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.