Olanzapine

Product NDC

0615-7670

11-digit product format

006157670

Labeler code

0615

Product ID

0615-7670_f1f82ae5-53d2-4cb5-a4bc-682d66082524

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Olanzapine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA076000

Marketing category

ANDA

Marketing start

2011-10-24

Marketing end

0000-00-00

Substance

OLANZAPINE

Active strength

3 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record