Alora

Product NDC

52544-884

11-digit product format

525440884

Labeler code

52544

Product ID

52544-884_0aa737e1-20d4-4ae4-b626-cd3e4940c7c4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Estradiol

Dosage form

PATCH

Route

TRANSDERMAL

Labeler

Actavis Pharma, Inc.

Application

NDA020655

Marketing category

NDA

Marketing start

2002-04-05

Marketing end

2020-12-21

Substance

ESTRADIOL

Active strength

0 mg/d

Pharmacologic classes

Estradiol Congeners [CS],Estrogen [EPC],Estrogen Receptor Agonists [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record