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Clonidine Hydrochloride

NDC 70069-044 · Somerset Therapeutics, LLC

Generic nameClonidine Hydrochloride
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)CLONIDINE HYDROCHLORIDE
Strength.1 mg/1
Pharmacologic classAdrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
Marketing categoryANDA

Packages

70069-044-01 — 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70069-044-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3016 — Clonidine Hydrochloride, 68071-3625 — clonidine hydrochloride, 68071-3987 — Clonidine hydrochloride, 68071-4545 — Clonidine hydrochloride, 68071-4661 — Clonidine Hydrochloride, 68180-606 — Clonidine Hydrochloride, 68788-7145 — Clonidine Hydrochloride, 68788-8080 — Clonidine Hydrochloride, 68788-8163 — Clonidine Hydrochloride, 68788-8494 — clonidine hydrochloride, 70518-1035 — Clonidine Hydrochloride, 70518-1060 — Clonidine Hydrochloride, 70518-1962 — Clonidine Hydrochloride, 70518-2203 — clonidine hydrochloride, 70518-3162 — clonidine hydrochloride, 70518-3295 — Clonidine Hydrochloride, 70518-4342 — Clonidine Hydrochloride, 70518-4357 — Clonidine Hydrochloride, 70518-4379 — Clonidine Hydrochloride, 71034-001 — Clonidine Hydrochloride, +126 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.