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Orange Book product · Generic (ANDA)

ROPIVACAINE HYDROCHLORIDE

ROPIVACAINE HYDROCHLORIDE

Generic (ANDA)ANDA 206166TE APRX INFORLIFE

At a glance

Jun 11, 2018

Approved

Generic (ANDA)

Application

AP

TE code

None

Listed patents

Key dates

  1. Approval

    FDA approval date of this drug product.

    Jun 11, 2018

    8 yr 2 mo ago

  2. Today

Pharmaceutical detail

Active ingredient

ROPIVACAINE HYDROCHLORIDE

Strength

1GM/200ML (5MG/ML)

Dosage form

SOLUTION

Route

INJECTION

TE code

AP

Application

ANDA 206166

Product number

004

Marketing status

RX

Reference listed drug (RLD)

No

Reference standard (RS)

No

Active-ingredient family

View full family

Generic (ANDA) of ROPIVACAINE HYDROCHLORIDE

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.