NDC 10135-667 – Prazosin Hydrochloride

Prazosin Hydrochloride 2 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC10135-667

Product details

Brand name
Prazosin Hydrochloride
Generic name
Prazosin Hydrochloride
Labeler
Marlex Pharmaceuticals Inc
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA210971
Marketed since
October 1, 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 (2)

Package NDCDescriptionSince
10135-667-01100 CAPSULE in 1 BOTTLE (10135-667-01)Oct 1, 2018
10135-667-101000 CAPSULE in 1 BOTTLE (10135-667-10)Oct 1, 2018

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