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Androgel
Androgel - 54569-5339-0 - (Testosterone)
Drug Information of Androgel
| 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) |
Labeler Information of Androgel
| 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 Information of Androgel
| Package NDC: | 54569-5339-0 |
| Package Description: | 150 g in 1 CARTON (54569-5339-0) |
NDC Information of Androgel
| NDC Code | 54569-5339-0 |
| Proprietary Name | Androgel |
| Package Description | 150 g in 1 CARTON (54569-5339-0) |
| 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] |
