Androderm

Product NDC
52544-077
11-digit product format
525440077
Labeler code
52544
Product ID
52544-077_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
4 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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
52544-077-30EA - Each52544-077fbdb63dc-2351-412a-badb-a8645b8d2f5e12012-07-24