NDC 67877-450 – Tamsulosin Hydrochloride

Tamsulosin Hydrochloride .4 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC67877-450

Product details

Brand name
Tamsulosin Hydrochloride
Generic name
Tamsulosin Hydrochloride
Labeler
Ascend Laboratories, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA207405
Marketed since
August 11, 2017
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
67877-450-01100 CAPSULE in 1 BOTTLE (67877-450-01)Aug 11, 2017
67877-450-05500 CAPSULE in 1 BOTTLE (67877-450-05)Aug 11, 2017
67877-450-101000 CAPSULE in 1 BOTTLE (67877-450-10)Aug 11, 2017
67877-450-3030 CAPSULE in 1 BOTTLE (67877-450-30)Aug 11, 2017
67877-450-3810 BLISTER PACK in 1 CARTON (67877-450-38) / 10 CAPSULE in 1 BLISTER PACK (67877-450-33)Aug 11, 2017
67877-450-6060 CAPSULE in 1 BOTTLE (67877-450-60)Aug 11, 2017

Recalls mentioning this NDC

Other Tamsulosin Hydrochloride products