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Orange Book product · Generic (ANDA)

DROXIDOPA

DROXIDOPA

Generic (ANDA)ANDA 211726TE ABRX ANNORA
View DROXIDOPA familyOpen on FDA Orange Book

At a glance

Aug 09, 2021

Approved

Generic (ANDA)

Application

AB

TE code

None

Listed patents

Key dates

  1. Approval

    FDA approval date of this drug product.

    Aug 09, 2021

    4 yr 11 mo ago

  2. Today

Pharmaceutical detail

Active ingredient

DROXIDOPA

Strength

100MG

Dosage form

CAPSULE

Route

ORAL

TE code

AB

Application

ANDA 211726

Product number

002

Marketing status

RX

Reference listed drug (RLD)

No

Reference standard (RS)

No

Active-ingredient family

View full family

Generic (ANDA) of DROXIDOPA

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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