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prazosin hydrochloride

NDC 70756-429 · Lifestar Pharma LLC

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

70756-429-11 — 100 CAPSULE in 1 BOTTLE (70756-429-11)

70756-429-12 — 1000 CAPSULE in 1 BOTTLE (70756-429-12)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-3271 — prazosin hydrochloride, 70518-3352 — Prazosin Hydrochloride, 70518-3669 — prazosin hydrochloride, 70518-3679 — prazosin hydrochloride, 70518-3928 — Prazosin hydrochloride, 70518-4263 — Prazosin hydrochloride, 70518-4288 — prazosin hydrochloride, 70518-4457 — Prazosin Hydrochloride, 70518-4489 — Prazosin Hydrochloride, 70518-4712 — prazosin hydrochloride, 70756-430 — 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, 71335-1401 — Prazosin Hydrochloride, 71335-1724 — prazosin hydrochloride, 71335-2311 — 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.