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Pramipexole dihydrochloride

NDC 68462-334, Pramipexole dihydrochloride, tablet, from Glenmark Pharmaceuticals Inc., USA.

Product NDC
68462-334
Status
Listed
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090781
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68462-334 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAMIPEXOLE DIHYDROCHLORIDE1.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68462-334-0568462033405500 TABLET in 1 BOTTLE (68462-334-05)
68462-334-116846203341110 BLISTER PACK in 1 CARTON (68462-334-11) / 10 TABLET in 1 BLISTER PACK
68462-334-906846203349090 TABLET in 1 BOTTLE (68462-334-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/44c336d2-01d1-4f13-bad9-549cdc3505ec

  • NADAC price for package 68462033490

    GET /v1/drugs/nadac/68462033490

Use it

Look up 68462-334 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68462-334 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68462-334. 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.