NDC 0093-4069 – Prazosin Hydrochloride

Prazosin Hydrochloride 5 mg/1 · Capsule · Oral

Human Prescription Drug 3 recalls

Product NDC0093-4069

Product details

Brand name
Prazosin Hydrochloride
Generic name
Prazosin Hydrochloride
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA071745
Marketed since
January 18, 2007
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
0093-4069-01100 CAPSULE in 1 BOTTLE (0093-4069-01)Feb 22, 2007
0093-4069-05500 CAPSULE in 1 BOTTLE (0093-4069-05)Jan 18, 2007
0093-4069-52250 CAPSULE in 1 BOTTLE (0093-4069-52)Feb 22, 2007

Recalls mentioning this NDC

Other Prazosin Hydrochloride products