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Prazosin Hydrochloride

NDC 70954-020 · ANI Pharmaceuticals, Inc.

Generic namePrazosin Hydrochloride
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PRAZOSIN HYDROCHLORIDE
Strength2 mg/1
Pharmacologic classAdrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

70954-020-10 — 100 CAPSULE in 1 BOTTLE (70954-020-10)

70954-020-20 — 1000 CAPSULE in 1 BOTTLE (70954-020-20)

70954-020-40 — 100 BLISTER PACK in 1 CARTON (70954-020-40) / 1 CAPSULE in 1 BLISTER PACK (70954-020-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 70756-440 — prazosin hydrochloride, 70954-019 — Prazosin Hydrochloride, 70954-021 — Prazosin Hydrochloride, 71205-585 — Prazosin Hydrochloride, 71335-1085 — Prazosin Hydrochloride, 71335-1401 — Prazosin Hydrochloride, 71335-1724 — prazosin hydrochloride, 71335-2311 — prazosin hydrochloride, 71335-2348 — prazosin hydrochloride, 71335-9648 — prazosin hydrochloride, 71610-693 — Prazosin Hydrochloride, 71610-694 — 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.