Androderm

Product NDC

52544-076

11-digit product format

525440076

Labeler code

52544

Product ID

52544-076_5e3d06a3-14c5-4c06-a414-09ebff3036a5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Testosterone

Dosage form

PATCH

Route

TRANSDERMAL

Labeler

Actavis Pharma, Inc.

Application

NDA020489

Marketing category

NDA

Marketing start

1995-09-29

Marketing end

2020-01-31

Substance

TESTOSTERONE

Active strength

2 mg/d

Pharmacologic classes

Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [CS]

DEA schedule

CIII

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record