Olanzapine

Product NDC

70518-0615

11-digit product format

705180615

Labeler code

70518

Product ID

70518-0615_8643994f-4e16-4572-e053-2991aa0a5b78

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Olanzapine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076255

Marketing category

ANDA

Marketing start

2017-07-12

Marketing end

0000-00-00

Substance

OLANZAPINE

Active strength

3 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record