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Orange Book product · Generic (ANDA)

ACYCLOVIR SODIUM

ACYCLOVIR SODIUM

Generic (ANDA)ANDA 203701TE APRX EUGIA PHARMA
View ACYCLOVIR SODIUM familyOpen on FDA Orange Book

At a glance

Oct 11, 2013

Approved

Generic (ANDA)

Application

AP

TE code

None

Listed patents

Key dates

  1. Approval

    FDA approval date of this drug product.

    Oct 11, 2013

    12 yr 10 mo ago

  2. Today

Pharmaceutical detail

Active ingredient

ACYCLOVIR SODIUM

Strength

EQ 50MG BASE/ML

Dosage form

INJECTABLE

Route

INJECTION

TE code

AP

Application

ANDA 203701

Product number

001

Marketing status

RX

Reference listed drug (RLD)

No

Reference standard (RS)

No

Active-ingredient family

View full family

Generic (ANDA) of ACYCLOVIR SODIUM

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.

Agent CTA Background

Your Next Submission Could Take 6+ Fewer Weeks and Cost $250K Less.

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