Assyro AI

Orange Book product · Brand (NDA)

DEPAKOTE CP

DIVALPROEX SODIUM

Brand (NDA)NDA 019794DISCN ABBOTT
View DIVALPROEX SODIUM familyOpen on FDA Orange Book

At a glance

Jul 11, 1990

Approved

Brand (NDA)

Application

Not listed

TE code

None

Listed patents

Key dates

  1. Approval

    FDA approval date of this drug product.

    Jul 11, 1990

    36 yr 6 mo ago

  2. Today

Pharmaceutical detail

Active ingredient

DIVALPROEX SODIUM

Strength

EQ 250MG BASE

Dosage form

TABLET, DELAYED RELEASE

Route

ORAL

TE code

Not listed

Application

NDA 019794

Product number

001

Marketing status

DISCN

Reference listed drug (RLD)

No

Reference standard (RS)

No

Active-ingredient family

View full family

This is a brand (NDA) product. Other products sharing this active 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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