Anastrozole

Product NDC

63672-0015

11-digit product format

636720015

Labeler code

63672

Product ID

63672-0015_5debd92c-9b60-475d-bf8b-b8cae30e43c6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Anastrozole

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Synthon Pharmaceuticals, Inc.

Application

ANDA078322

Marketing category

ANDA

Marketing start

2010-06-28

Marketing end

0000-00-00

Substance

ANASTROZOLE

Active strength

1 mg/1

Pharmacologic classes

Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record