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: 59651-233_2b75c20c-9dcc-4a63-854a-e9cdd2d7c1fb
Product NDC: 59651-233
Form: TABLET
Composition / generic term: Clonidine Hydrochloride
Labeler: Aurobindo Pharma Limited
Marketing category: ANDA
Marketing start / end (source format): 20210602
Source listing expiry: 20261231

Source-listed ingredients

CLONIDINE HYDROCHLORIDE — .2 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET in 1 BOTTLE (59651-233-01) · 59651-233-01
500 TABLET in 1 BOTTLE (59651-233-05) · 59651-233-05

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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