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Clonidine Hydrochloride

NDC 71034-001, Clonidine Hydrochloride, tablet, extended release, from Xiamen LP Pharmaceutical Co., Ltd..

Product NDC
71034-001
Status
Listed
Labeler
Xiamen LP Pharmaceutical Co., Ltd.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209757
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71034-001 \
  -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
71034-001-607103400016060 TABLET, EXTENDED RELEASE in 1 BOTTLE (71034-001-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7676af27-4d8f-49c4-a50f-6b0892e73c8f

Use it

Look up 71034-001 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71034-001 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71034-001. 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.