NDC 70954-020 – Prazosin Hydrochloride

Prazosin Hydrochloride 2 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC70954-020

Product details

Brand name
Prazosin Hydrochloride
Generic name
Prazosin Hydrochloride
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA210971
Marketed since
October 3, 2018
Listing expires
December 31, 2027
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
70954-020-10100 CAPSULE in 1 BOTTLE (70954-020-10)Oct 3, 2018
70954-020-201000 CAPSULE in 1 BOTTLE (70954-020-20)Oct 3, 2018
70954-020-40100 BLISTER PACK in 1 CARTON (70954-020-40) / 1 CAPSULE in 1 BLISTER PACK (70954-020-30)Apr 13, 2021

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