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clonidine hydrochloride

NDC 83939-0006, clonidine hydrochloride, tablet, from VERITYRX, LLC.

Product NDC
83939-0006
Status
Listed
Labeler
VERITYRX, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078895
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/83939-0006 \
  -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
83939-0006-1839390006011 TABLET in 1 POUCH (83939-0006-1)
83939-0006-28393900060250 POUCH in 1 BOX, UNIT-DOSE (83939-0006-2) / 1 TABLET in 1 POUCH
83939-0006-383939000603100 POUCH in 1 BOX, UNIT-DOSE (83939-0006-3) / 1 TABLET in 1 POUCH

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/427939a4-6bbf-0d80-e063-6294a90aa2a0

Use it

Look up 83939-0006 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/83939-0006 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 83939-0006. 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.