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AXIRON
AXIRON - 0002-1975-61 - (testosterone)
Drug Information of AXIRON
| 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) |
Labeler Information of AXIRON
| 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 Information of AXIRON
| Package NDC: | 0002-1975-61 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0002-1975-61) > 90 mL in 1 BOTTLE, WITH APPLICATOR |
NDC Information of AXIRON
| NDC Code | 0002-1975-61 |
| Proprietary Name | AXIRON |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0002-1975-61) > 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] |
