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Terazosin

NDC 70518-0342 · REMEDYREPACK INC.

Generic nameTerazosin Hydrochloride
Dosage formCAPSULE
RouteORAL
Active ingredient(s)TERAZOSIN HYDROCHLORIDE
Strength1 mg/1
Pharmacologic classAdrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

70518-0342-0 — 30 CAPSULE in 1 BLISTER PACK (70518-0342-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69292-201 — Terazosin Hydrochloride, 69292-202 — Terazosin Hydrochloride, 69292-203 — Terazosin Hydrochloride, 69292-204 — Terazosin Hydrochloride, 69452-330 — Terazosin, 69452-331 — Terazosin, 69452-332 — Terazosin, 69452-333 — Terazosin, 70518-0074 — Terazosin Hydrochloride, 70518-0317 — Terazosin Hydrochloride, 70518-3193 — terazosin, 70518-4545 — Terazosin, 70954-592 — Terazosin, 71335-3059 — Terazosin, 71335-3123 — Terazosin, 71335-3131 — Terazosin, 71335-9607 — terazosin, 71610-478 — Terazosin Hydrochloride, 71610-503 — Terazosin Hydrochloride, 71610-510 — Terazosin Hydrochloride, +62 more

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