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Clonidine Hydrochloride

NDC 70069-044, Clonidine Hydrochloride, tablet, extended release, from Somerset Therapeutics, LLC.

Product NDC
70069-044
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211433
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-044 \
  -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
70069-044-017006900440160 TABLET, EXTENDED RELEASE in 1 BOTTLE (70069-044-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1b4fb182-8194-4fdd-bf9b-f7e60e734179

  • NADAC price for package 70069004401

    GET /v1/drugs/nadac/70069004401

Use it

Look up 70069-044 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-044 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-044. 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.