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
- 70069-044_b1e7ffe5-7d5f-4e02-a9c9-3d9ad3fac23e
- Product NDC
- 70069-044
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Clonidine Hydrochloride
- Labeler
- Somerset Therapeutics, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250304
- Source listing expiry
- 20261231
Source-listed ingredients
- CLONIDINE HYDROCHLORIDE — .1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70069-044-01) · 70069-044-01
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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