Pramipexole dihydrochloride

NDC 68462-331, Pramipexole dihydrochloride, tablet, from Glenmark Pharmaceuticals Inc., USA.

Product NDC: 68462-331
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/68462-331 \
  -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 NDC	NDC-11	Package
68462-331-05	68462033105	500 TABLET in 1 BOTTLE (68462-331-05)
68462-331-11	68462033111	10 BLISTER PACK in 1 CARTON (68462-331-11) / 10 TABLET in 1 BLISTER PACK
68462-331-90	68462033190	90 TABLET in 1 BOTTLE (68462-331-90)

Linked data

RxNorm, label and prices

RxNorm concepts

859040pramipexole dihydrochloride 0.25 MG Oral Tablet (SCD)

Related lookups

FDA label sections
GET /v1/drugs/labels/44c336d2-01d1-4f13-bad9-549cdc3505ec
NADAC price for package 68462033190
GET /v1/drugs/nadac/68462033190

Use it

Look up 68462-331 from code or an agent

curl

curl https://api.healthcare.dev/v1/drugs/ndc/68462-331 \
  -H "Authorization: Bearer $HDEV_API_KEY"

MCP prompt

Using the healthcare.dev MCP server, look up NDC 68462-331. 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.