Ozurdex 0.7 mg implant

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Allergan, Inc. names for other drugs.

Recalls

• Dec 20, 2018 · Class II · Allergan, PLC.
  GMP Deviations: A silicone particulate was noted in Ozurdex.
  Lots: E78689, exp. date 06/21/2019 E78726, exp. date 06/29/2019 E78729, exp. date 07/01/2019 E78894, exp. date 08/09/2019 E79157, exp. date 09/05/2019 E79233, exp. date 09/15/2019 E79366, exp. date 10/06/2019 E79891, exp. date 12/07/2019 E80122, exp. date 01/18/2020 E80216, exp. d…

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Dexamethasone: every company that makes it

Form

implant, intravitreal

Strength

0.7 mg

Approval

NDA NDA022315

On the market since

Sep 1, 2009

Package NDCs

0023-3348-07 0023-3348-08

Official label

DailyMed (National Library of Medicine), updated Mar 11, 2026

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?