Skip to main content

Prazosin Hydrochloride

NDC 70518-3352 · REMEDYREPACK INC.

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

70518-3352-0 — 100 POUCH in 1 BOX (70518-3352-0) / 1 CAPSULE in 1 POUCH (70518-3352-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-8742 — Prazosin Hydrochloride, 70010-084 — Prazosin Hydrochloride, 70010-085 — Prazosin Hydrochloride, 70010-086 — Prazosin Hydrochloride, 70377-066 — Prazosin hydrochloride, 70377-067 — Prazosin hydrochloride, 70377-068 — Prazosin hydrochloride, 70518-1443 — prazosin hydrochloride, 70518-2178 — Prazosin Hydrochloride, 70518-3271 — prazosin hydrochloride, 70518-3669 — prazosin hydrochloride, 70518-3679 — prazosin hydrochloride, 70518-3928 — Prazosin hydrochloride, 70518-4263 — Prazosin hydrochloride, 70518-4288 — prazosin hydrochloride, 70518-4457 — Prazosin Hydrochloride, 70518-4489 — Prazosin Hydrochloride, 70518-4712 — prazosin hydrochloride, 70756-429 — prazosin hydrochloride, 70756-430 — 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.