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Clonidine Hydrochloride

NDC 51655-353, Clonidine Hydrochloride, tablet, from Northwind Health Company, LLC.

Product NDC
51655-353
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA070974
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-353 \
  -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
51655-353-525165503535230 TABLET in 1 BOTTLE, DISPENSING (51655-353-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/66dc3cf0-d6bd-436c-9a7f-7477575b3260

Use it

Look up 51655-353 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-353 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-353. 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.