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Prazosin HCL

NDC 72189-436 · Direct_Rx

Generic namePrazosin HCL
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PRAZOSIN HYDROCHLORIDE
Strength1 mg/1
Pharmacologic classAdrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

72189-436-30 — 30 CAPSULE in 1 BOTTLE (72189-436-30)

72189-436-60 — 60 CAPSULE in 1 BOTTLE (72189-436-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-1401 — Prazosin Hydrochloride, 71335-1724 — prazosin hydrochloride, 71335-2311 — prazosin hydrochloride, 71335-2348 — prazosin hydrochloride, 71335-9648 — prazosin hydrochloride, 71610-693 — Prazosin Hydrochloride, 71610-694 — Prazosin Hydrochloride, 71610-829 — Prazosin Hydrochloride, 71610-980 — Prazosin Hydrochloride, 71610-981 — Prazosin Hydrochloride, 72189-470 — Prazosin HCL, 72189-540 — Prazosin HCL, 72205-275 — prazosin hydrochloride, 72205-276 — prazosin hydrochloride, 72205-277 — prazosin hydrochloride, 76282-721 — Prazosin Hydrochloride, 76282-722 — Prazosin Hydrochloride, 76282-723 — Prazosin Hydrochloride, 76420-523 — prazosin hydrochloride, 76420-525 — prazosin hydrochloride, +89 more

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