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Clonidine Hydrochloride

NDC 59651-232, Clonidine Hydrochloride, tablet, from Aurobindo Pharma Limited.

Product NDC
59651-232
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA070886
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-232 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CLONIDINE HYDROCHLORIDE.1 mg/1

Pharmacologic classes

Adrenergic alpha2-Agonists [MoA]; Central alpha-2 Adrenergic Agonist [EPC]

Package NDCNDC-11Package
59651-232-0159651023201100 TABLET in 1 BOTTLE (59651-232-01)
59651-232-99596510232991000 TABLET in 1 BOTTLE (59651-232-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2b75c20c-9dcc-4a63-854a-e9cdd2d7c1fb

  • NADAC price for package 59651023201

    GET /v1/drugs/nadac/59651023201

  • NADAC price for package 59651023299

    GET /v1/drugs/nadac/59651023299

Use it

Look up 59651-232 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-232 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-232. 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.