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Orange Book product · Generic (ANDA)

OCTREOTIDE ACETATE

OCTREOTIDE ACETATE

Generic (ANDA)ANDA 091041TE APRX SAGENT PHARMS INC

At a glance

Nov 12, 2013

Approved

Generic (ANDA)

Application

AP

TE code

None

Listed patents

Key dates

  1. Approval

    FDA approval date of this drug product.

    Nov 12, 2013

    12 yr 9 mo ago

  2. Today

Pharmaceutical detail

Active ingredient

OCTREOTIDE ACETATE

Strength

EQ 0.2MG BASE/ML

Dosage form

INJECTABLE

Route

INJECTION

TE code

AP

Application

ANDA 091041

Product number

001

Marketing status

RX

Reference listed drug (RLD)

No

Reference standard (RS)

No

Active-ingredient family

View full family

Generic (ANDA) of OCTREOTIDE ACETATE

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.