NDC 71335-1401 – Prazosin Hydrochloride

Prazosin Hydrochloride 1 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1401

Product details

Brand name
Prazosin Hydrochloride
Generic name
Prazosin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA210971
Marketed since
October 3, 2018
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
71335-1401-130 CAPSULE in 1 BOTTLE (71335-1401-1)Feb 9, 2022
71335-1401-2100 CAPSULE in 1 BOTTLE (71335-1401-2)Feb 9, 2022
71335-1401-360 CAPSULE in 1 BOTTLE (71335-1401-3)Feb 9, 2022
71335-1401-428 CAPSULE in 1 BOTTLE (71335-1401-4)Feb 9, 2022
71335-1401-590 CAPSULE in 1 BOTTLE (71335-1401-5)Feb 9, 2022

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