Flomax

Product NDC

70518-0518

11-digit product format

705180518

Labeler code

70518

Product ID

70518-0518_85942785-7550-75ab-e053-2a91aa0afe68

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

tamsulosin hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA020579

Marketing category

NDA

Marketing start

2017-09-13

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