Letrozole

Product NDC

68084-803

11-digit product format

680840803

Labeler code

68084

Product ID

68084-803_66d8523c-2979-59e5-e053-2a91aa0a341f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Letrozole

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

American Health Packaging

Application

ANDA091303

Marketing category

ANDA

Marketing start

2014-07-31

Marketing end

2019-03-31

Substance

LETROZOLE

Active strength

3 mg/1

Pharmacologic classes

Aromatase Inhib

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record