United States · FDA National Drug Code directory
clonidine hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 83939-0005_42788b2f-2fbc-d9f8-e063-6294a90aa08e
- Product NDC
- 83939-0005
- Form
- TABLET
- Composition / generic term
- Clonidine Hydrochloride
- Labeler
- VERITYRX, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160503
- Source listing expiry
- 20261231
Source-listed ingredients
- CLONIDINE HYDROCHLORIDE — .1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TABLET in 1 POUCH (83939-0005-1) · 83939-0005-1
- 50 POUCH in 1 BOX, UNIT-DOSE (83939-0005-2) / 1 TABLET in 1 POUCH · 83939-0005-2
- 100 POUCH in 1 BOX, UNIT-DOSE (83939-0005-3) / 1 TABLET in 1 POUCH · 83939-0005-3
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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