Olanzapine

Product NDC
0615-8246
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Olanzapine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Application
ANDA202862
Marketing category
ANDA
Substance
OLANZAPINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
0615-8246-3930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8246-39) 2018-11-02NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
OlanzapineNCS HealthCare of KY, LLC dba Vangard Labs2025-03-03HUMAN PRESCRIPTION DRUG LABEL13