NDC 62756-160 – Tamsulosin Hydrochloride

Tamsulosin Hydrochloride .4 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC62756-160

Product details

Brand name
Tamsulosin Hydrochloride
Generic name
Tamsulosin Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA090931
Marketed since
July 15, 2010
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
62756-160-08100 CAPSULE in 1 BOTTLE (62756-160-08)Jul 15, 2010
62756-160-13500 CAPSULE in 1 BOTTLE (62756-160-13)Jul 15, 2010
62756-160-181000 CAPSULE in 1 BOTTLE (62756-160-18)Jul 15, 2010
62756-160-8190 CAPSULE in 1 BOTTLE (62756-160-81)Jul 15, 2010
62756-160-8330 CAPSULE in 1 BOTTLE (62756-160-83)Jul 15, 2010
62756-160-88100 CAPSULE in 1 BOTTLE (62756-160-88)Jul 15, 2010

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