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Prazosin Hydrochloride

NDC 59651-273 · Aurobindo Pharma Limited

Generic namePrazosin Hydrochloride
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PRAZOSIN HYDROCHLORIDE
Strength5 mg/1
Pharmacologic classAdrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

59651-273-01 — 100 CAPSULE in 1 BOTTLE (59651-273-01)

59651-273-25 — 250 CAPSULE in 1 BOTTLE (59651-273-25)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

48433-086 — prazosin hydrochloride, 50090-5695 — Prazosin Hydrochloride, 51079-630 — prazosin hydrochloride, 51079-631 — prazosin hydrochloride, 51079-632 — prazosin hydrochloride, 55154-4156 — Prazosin Hydrochloride, 55154-8181 — Prazosin Hydrochloride, 55289-536 — prazosin hydrochloride, 59651-271 — Prazosin Hydrochloride, 59651-272 — Prazosin Hydrochloride, 60687-572 — Prazosin Hydrochloride, 60760-820 — prazosin hydrochloride, 60760-821 — prazosin hydrochloride, 62332-691 — PRAZOSIN HYDROCHLORIDE, 62332-692 — PRAZOSIN HYDROCHLORIDE, 62332-693 — PRAZOSIN HYDROCHLORIDE, 63629-8750 — Prazosin Hydrochloride, 63629-8756 — Prazosin Hydrochloride, 66993-431 — prazosin hydrochloride, 66993-432 — 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.