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PRAZOSIN HYDROCHLORIDE

NDC 62332-691 · Alembic Pharmaceuticals Inc.

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

Packages

62332-691-31 — 100 CAPSULE in 1 BOTTLE (62332-691-31)

62332-691-61 — 250 CAPSULE in 1 BOTTLE (62332-691-61)

62332-691-91 — 1000 CAPSULE in 1 BOTTLE (62332-691-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51079-632 — prazosin hydrochloride, 55154-4156 — Prazosin Hydrochloride, 55154-8181 — Prazosin Hydrochloride, 55289-536 — prazosin hydrochloride, 59651-271 — Prazosin Hydrochloride, 59651-272 — Prazosin Hydrochloride, 59651-273 — Prazosin Hydrochloride, 60687-572 — Prazosin Hydrochloride, 60760-820 — prazosin hydrochloride, 60760-821 — 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, 66993-433 — prazosin hydrochloride, 67046-0504 — Prazosin Hydrochloride, 67046-0680 — Prazosin Hydrochloride, 67046-0781 — 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.