NDC 0378-1101 – Prazosin Hydrochloride

Prazosin Hydrochloride 1 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC0378-1101

Product details

Brand name
Prazosin Hydrochloride
Generic name
Prazosin hydrochloride
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA072575
Marketed since
February 28, 1989
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0378-1101-01100 CAPSULE in 1 BOTTLE, PLASTIC (0378-1101-01)Feb 28, 1989
0378-1101-101000 CAPSULE in 1 BOTTLE, PLASTIC (0378-1101-10)Feb 28, 1989

Recalls mentioning this NDC

Other Prazosin Hydrochloride products