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Prazosin Hydrochloride

NDC 71335-1401 · Bryant Ranch Prepack

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

71335-1401-1 — 30 CAPSULE in 1 BOTTLE (71335-1401-1)

71335-1401-2 — 100 CAPSULE in 1 BOTTLE (71335-1401-2)

71335-1401-3 — 60 CAPSULE in 1 BOTTLE (71335-1401-3)

71335-1401-4 — 28 CAPSULE in 1 BOTTLE (71335-1401-4)

71335-1401-5 — 90 CAPSULE in 1 BOTTLE (71335-1401-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4489 — Prazosin Hydrochloride, 70518-4712 — prazosin hydrochloride, 70756-429 — prazosin hydrochloride, 70756-430 — prazosin hydrochloride, 70756-440 — prazosin hydrochloride, 70954-019 — Prazosin Hydrochloride, 70954-020 — Prazosin Hydrochloride, 70954-021 — Prazosin Hydrochloride, 71205-585 — Prazosin Hydrochloride, 71335-1085 — 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, 71610-829 — Prazosin Hydrochloride, 71610-980 — Prazosin Hydrochloride, 71610-981 — Prazosin Hydrochloride, 72189-436 — Prazosin HCL, +89 more

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