Prazosin

NDC 0527-4180 · Lannett Company, Inc.

Generic namePrazosin

Dosage formCAPSULE

RouteORAL

Active ingredient(s)PRAZOSIN HYDROCHLORIDE

Strength1 mg/1

Pharmacologic classAdrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]

Marketing categoryANDA

Packages

0527-4180-37 — 100 CAPSULE in 1 BOTTLE (0527-4180-37)

0527-4180-43 — 1000 CAPSULE in 1 BOTTLE (0527-4180-43)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0093-4067 — Prazosin Hydrochloride, 0093-4068 — Prazosin Hydrochloride, 0093-4069 — Prazosin Hydrochloride, 0378-1101 — prazosin hydrochloride, 0378-2302 — prazosin hydrochloride, 0378-3205 — prazosin hydrochloride, 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, 10135-666 — 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, +89 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.