Olanzapine

Product NDC

70518-1206

11-digit product format

705181206

Labeler code

70518

Product ID

70518-1206_909d74e4-3727-6885-e053-2995a90a0d9d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Olanzapine

Dosage form

TABLET, ORALLY DISINTEGRATING

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA091265

Marketing category

ANDA

Marketing start

2018-05-15

Marketing end

0000-00-00

Substance

OLANZAPINE

Active strength

5 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record