Tamsulosin Hydrochloride

Product NDC

51079-294

11-digit product format

510790294

Labeler code

51079

Product ID

51079-294_7d8ecf17-1f51-f4ec-e053-2991aa0a0f4f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

tamsulosin hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA090408

Marketing category

ANDA

Marketing start

2010-05-07

Marketing end

0000-00-00

Substance

TAMSULOSIN HYDROCHLORIDE

Active strength

0 mg/1

Pharmacologic classes

Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record