Skip to main content

Prazosin Hydrochloride

NDC 0093-4069 · Teva Pharmaceuticals USA, 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

0093-4069-01 — 100 CAPSULE in 1 BOTTLE (0093-4069-01)

0093-4069-05 — 500 CAPSULE in 1 BOTTLE (0093-4069-05)

0093-4069-52 — 250 CAPSULE in 1 BOTTLE (0093-4069-52)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0093-4067 — Prazosin Hydrochloride, 0093-4068 — Prazosin Hydrochloride, 0378-1101 — prazosin hydrochloride, 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, 10135-666 — 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 August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.