Product NDC: | 0002-1975 |
Proprietary Name: | AXIRON |
Non Proprietary Name: | testosterone |
Active Ingredient(s): | 30 mg/1.5mL & nbsp; testosterone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0002-1975 |
Labeler Name: | Eli Lilly and Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022504 |
Marketing Category: | NDA |
Start Marketing Date: | 20101201 |
Package NDC: | 0002-1975-90 |
Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0002-1975-90) > 90 mL in 1 BOTTLE, WITH APPLICATOR |
NDC Code | 0002-1975-90 |
Proprietary Name | AXIRON |
Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0002-1975-90) > 90 mL in 1 BOTTLE, WITH APPLICATOR |
Product NDC | 0002-1975 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | testosterone |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20101201 |
Marketing Category Name | NDA |
Labeler Name | Eli Lilly and Company |
Substance Name | TESTOSTERONE |
Strength Number | 30 |
Strength Unit | mg/1.5mL |
Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |