Orange Book product · Brand (NDA)

TENEX

GUANFACINE HYDROCHLORIDE

Brand (NDA)NDA 019032DISCN PROMIUS PHARMA

View GUANFACINE HYDROCHLORIDE family Open on FDA Orange Book

At a glance

Oct 27, 1986

Approved

Brand (NDA)

Application

Not listed

TE code

None

Listed patents

Key dates

Approval
FDA approval date of this drug product.
Oct 27, 1986
40 yr 3 mo ago
Today

Pharmaceutical detail

Active ingredient

GUANFACINE HYDROCHLORIDE

Strength

EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Dosage form

TABLET

Route

ORAL

TE code

Not listed

Application

NDA 019032

Product number

001

Marketing status

DISCN

Reference listed drug (RLD)

Yes

Reference standard (RS)

Active-ingredient family

View full family

This is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.

Listed patents

No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.

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