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PRAZOSIN HYDROCHLORIDE

NDC 46708-693 · Alembic Pharmaceuticals Limited

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

46708-693-31 — 100 CAPSULE in 1 BOTTLE (46708-693-31)

46708-693-61 — 250 CAPSULE in 1 BOTTLE (46708-693-61)

46708-693-91 — 1000 CAPSULE in 1 BOTTLE (46708-693-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 48433-084 — prazosin hydrochloride, 48433-085 — prazosin hydrochloride, 48433-086 — prazosin hydrochloride, 50090-5695 — Prazosin Hydrochloride, 51079-630 — prazosin hydrochloride, 51079-631 — prazosin hydrochloride, 51079-632 — prazosin hydrochloride, 55154-4156 — Prazosin Hydrochloride, 55154-8181 — Prazosin Hydrochloride, 55289-536 — 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.