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Prazosin Hydrochloride

NDC 10135-666 · Marlex 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

10135-666-01 — 100 CAPSULE in 1 BOTTLE (10135-666-01)

10135-666-10 — 1000 CAPSULE in 1 BOTTLE (10135-666-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0378-2302 — prazosin hydrochloride, 0378-3205 — prazosin hydrochloride, 0527-4180 — Prazosin, 0527-4181 — Prazosin, 0527-4182 — Prazosin, 0615-8519 — Prazosin Hydrochloride, 0615-8520 — Prazosin Hydrochloride, 0904-7020 — Prazosin Hydrochloride, 0904-7021 — Prazosin Hydrochloride, 0904-7022 — Prazosin Hydrochloride, 10135-667 — Prazosin Hydrochloride, 10135-668 — Prazosin Hydrochloride, 43063-248 — prazosin hydrochloride, 43063-260 — prazosin hydrochloride, 46708-691 — PRAZOSIN HYDROCHLORIDE, 46708-692 — PRAZOSIN HYDROCHLORIDE, 46708-693 — PRAZOSIN HYDROCHLORIDE, 48433-084 — prazosin hydrochloride, 48433-085 — prazosin hydrochloride, 48433-086 — 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.