LETROZOLE

Product NDC

62756-511

11-digit product format

627560511

Labeler code

62756

Product ID

62756-511_caa42adc-a41b-486c-8b97-9e8ed3213bda

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

LETROZOLE

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Sun Pharmaceutical Indust

Application

ANDA091466

Marketing category

ANDA

Marketing start

2015-09-09

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