NDC 33342-159 – Tamsulosin Hydrochloride

Tamsulosin Hydrochloride .4 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC33342-159

Product details

Brand name
Tamsulosin Hydrochloride
Generic name
Tamsulosin Hydrochloride
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA204645
Marketed since
January 25, 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 (5)

Package NDCDescriptionSince
33342-159-0730 CAPSULE in 1 BOTTLE (33342-159-07)Jan 25, 2017
33342-159-11100 CAPSULE in 1 BOTTLE (33342-159-11)Jan 25, 2017
33342-159-1210 BLISTER PACK in 1 CARTON (33342-159-12) / 10 CAPSULE in 1 BLISTER PACKJan 25, 2017
33342-159-15500 CAPSULE in 1 BOTTLE (33342-159-15)Jan 25, 2017
33342-159-441000 CAPSULE in 1 BOTTLE (33342-159-44)Jan 25, 2017

Recalls mentioning this NDC

Other Tamsulosin Hydrochloride products