Product NDC: | 54569-5339 |
Proprietary Name: | Androgel |
Non Proprietary Name: | Testosterone |
Active Ingredient(s): | 10 mg/g & nbsp; Testosterone |
Administration Route(s): | TRANSDERMAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-5339 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021015 |
Marketing Category: | NDA |
Start Marketing Date: | 20110314 |
Package NDC: | 54569-5339-1 |
Package Description: | 300 g in 1 CARTON (54569-5339-1) |
NDC Code | 54569-5339-1 |
Proprietary Name | Androgel |
Package Description | 300 g in 1 CARTON (54569-5339-1) |
Product NDC | 54569-5339 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Testosterone |
Dosage Form Name | GEL |
Route Name | TRANSDERMAL |
Start Marketing Date | 20110314 |
Marketing Category Name | NDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | TESTOSTERONE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |