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Orange Book product · Brand (NDA)

SUFENTA PRESERVATIVE FREE

SUFENTANIL CITRATE

Brand (NDA)NDA 019050TE APRX RISING
View SUFENTANIL CITRATE familyOpen on FDA Orange Book

At a glance

May 04, 1984

Approved

Brand (NDA)

Application

AP

TE code

None

Listed patents

Key dates

  1. Approval

    FDA approval date of this drug product.

    May 04, 1984

    42 yr 9 mo ago

  2. Today

Pharmaceutical detail

Active ingredient

SUFENTANIL CITRATE

Strength

EQ 0.05MG BASE/ML

Dosage form

INJECTABLE

Route

INJECTION

TE code

AP

Application

NDA 019050

Product number

001

Marketing status

RX

Reference listed drug (RLD)

Yes

Reference standard (RS)

Yes

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.

Agent CTA Background

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