NDC 71335-9648 – Prazosin hydrochloride

Prazosin Hydrochloride 1 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-9648

Product details

Brand name
Prazosin hydrochloride
Generic name
Prazosin hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA215697
Marketed since
January 3, 2023
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Prazosin Hydrochloride →

Package NDC codes (5)

Package NDCDescriptionSince
71335-9648-130 CAPSULE in 1 BOTTLE (71335-9648-1)Feb 21, 2023
71335-9648-2100 CAPSULE in 1 BOTTLE (71335-9648-2)Feb 21, 2023
71335-9648-360 CAPSULE in 1 BOTTLE (71335-9648-3)Feb 21, 2023
71335-9648-428 CAPSULE in 1 BOTTLE (71335-9648-4)Feb 21, 2023
71335-9648-590 CAPSULE in 1 BOTTLE (71335-9648-5)Feb 21, 2023

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