Olanzapine

Product NDC

61786-005

11-digit product format

617860005

Labeler code

61786

Product ID

61786-005_741fe96a-7a49-5d85-e053-2991aa0a9d22

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Olanzapine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076133

Marketing category

ANDA

Marketing start

2014-08-07

Marketing end

0000-00-00

Substance

OLANZAPINE

Active strength

20 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record