Olanzapine

Product NDC

70518-0149

11-digit product format

705180149

Labeler code

70518

Product ID

70518-0149_9f5f0076-399f-5add-e053-2995a90abc4d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Olanzapine

Dosage form

TABLET, ORALLY DISINTEGRATING

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA203044

Marketing category

ANDA

Marketing start

2017-01-19

Marketing end

0000-00-00

Substance

OLANZAPINE

Active strength

15 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record