Tamsulosin Hydrochloride

Product NDC

70518-1208

11-digit product format

705181208

Labeler code

70518

Product ID

70518-1208_825b68cf-9663-654b-e053-2a91aa0a7e37

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tamsulosin Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA207405

Marketing category

ANDA

Marketing start

2018-05-15

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

2020-12-31

Current FDA listing

Historical FDA.report record