Olanzapine

Product NDC

50268-609

11-digit product format

502680609

Labeler code

50268

Product ID

50268-609_9c98792f-c143-2bbd-e053-2995a90af659

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Olanzapine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

AvPAK

Application

ANDA090798

Marketing category

ANDA

Marketing start

2016-10-12

Marketing end

0000-00-00

Substance

OLANZAPINE

Active strength

3 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record