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