Olanzapine

Product NDC

0615-7673

11-digit product format

006157673

Labeler code

0615

Product ID

0615-7673_f8640667-468a-4ad3-892b-9ccd40f6a591

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Olanzapine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA076133

Marketing category

ANDA

Marketing start

2011-10-24

Marketing end

0000-00-00

Substance

OLANZAPINE

Active strength

20 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record