NDC 70518-3669 – Prazosin hydrochloride

Prazosin Hydrochloride 1 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC70518-3669

Product details

Brand name
Prazosin hydrochloride
Generic name
Prazosin hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA215697
Marketed since
March 3, 2023
Listing expires
December 31, 2027
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
70518-3669-430 CAPSULE in 1 BOTTLE, PLASTIC (70518-3669-4)Aug 27, 2025
70518-3669-5100 POUCH in 1 BOX (70518-3669-5) / 1 CAPSULE in 1 POUCH (70518-3669-6)Feb 10, 2026

Other Prazosin Hydrochloride products