← FDA DRUG APPROVALS

FDA NDA · NDA022173

ZYPREXA RELPREVV

olanzapine pamoate

Sponsor: CHEPLAPHARM

APPLICATION
NDA022173
TYPE
NDA
ORIGINAL APPROVAL
2009-12-11
LATEST ACTION
2026-05-07
ROUTE
INTRAMUSCULAR
DOSAGE FORM
SUSPENSION, EXTENDED RELEASE
MARKETING STATUS
Prescription

Products

ZYPREXA RELPREVV · ReferencePrescription
OLANZAPINE PAMOATE EQ 405MG BASE/VIAL · SUSPENSION, EXTENDED RELEASE · INTRAMUSCULAR
ZYPREXA RELPREVV · ReferencePrescription
OLANZAPINE PAMOATE EQ 210MG BASE/VIAL · SUSPENSION, EXTENDED RELEASE · INTRAMUSCULAR
ZYPREXA RELPREVV · ReferencePrescription
OLANZAPINE PAMOATE EQ 300MG BASE/VIAL · SUSPENSION, EXTENDED RELEASE · INTRAMUSCULAR

Approval history

2026-05-07Labeling · Supplement 43 · standardLetterAP
2026-05-07REMS · Supplement 40LetterAP
2026-01-30Labeling · Supplement 50 · standardLetterAP
2025-01-22Labeling · Supplement 47 · standardLabelAP
2021-04-28REMS · Supplement 39LetterAP
2021-01-13Labeling · Supplement 37 · standardLetterAP
2020-04-23Labeling · Supplement 34 · standardLabelAP
2020-04-22REMS · Supplement 35LetterAP
2020-04-21Labeling · Supplement 36 · 901 requiredLetterAP
2019-10-22Labeling · Supplement 30 · standardLetterAP
2019-04-11REMS · Supplement 32LabelAP
2018-03-27Labeling · Supplement 29 · standardLabelAP
2017-11-30REMS · Supplement 27LabelAP
2017-02-23Labeling · Supplement 28 · 901 requiredLabelAP
2017-02-23Labeling · Supplement 26 · standardLabelAP
2016-10-06Labeling · Supplement 25 · 901 requiredLetterAP
2015-12-23Manufacturing (CMC) · Supplement 19 · standardAP
2015-09-17Labeling · Supplement 24 · standardLetterAP
2015-07-23Labeling · Supplement 17 · standardLabelAP
2014-12-19Labeling · Supplement 15 · standardLabelAP
2014-10-30REMS · Supplement 23LabelAP
2014-02-18Manufacturing (CMC) · Supplement 20 · standardAP
2013-03-27REMS · Supplement 18LabelAP
2012-08-03REMS · Supplement 10LetterAP
2012-08-03REMS · Supplement 8LetterAP
2012-08-03REMS · Supplement 14LabelAP
2010-12-01Labeling · Supplement 9 · 901 requiredLabelAP
2010-07-08REMS · Supplement 4LetterAP
2010-05-27Labeling · Supplement 6 · unknownLabelAP
2010-05-27Labeling · Supplement 3 · unknownLabelAP
2010-04-27Labeling · Supplement 2 · unknownLetterAP
2009-12-11Type 3 - New Dosage Form · Original · standardOther Important Information from FDAAP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

Pharma industryGMP disciplineFDA drug shortagesFDA enforcement & recalls

Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

Weekly Briefing

Get the Weekly GxP Briefing

Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.

Read a past issue →