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Androderm
Androderm - 52544-469-60 - (Testosterone)
Drug Information of Androderm
| Product NDC: | 52544-469 |
| Proprietary Name: | Androderm |
| Non Proprietary Name: | Testosterone |
| Active Ingredient(s): | 2.5 mg/d & nbsp; Testosterone |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Androderm
| Product NDC: | 52544-469 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020489 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19950929 |
Package Information of Androderm
| Package NDC: | 52544-469-60 |
| Package Description: | 60 POUCH in 1 CARTON (52544-469-60) > 1 PATCH in 1 POUCH > 1 d in 1 PATCH |
NDC Information of Androderm
| NDC Code | 52544-469-60 |
| Proprietary Name | Androderm |
| Package Description | 60 POUCH in 1 CARTON (52544-469-60) > 1 PATCH in 1 POUCH > 1 d in 1 PATCH |
| Product NDC | 52544-469 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Testosterone |
| Dosage Form Name | PATCH |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 19950929 |
| Marketing Category Name | NDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | TESTOSTERONE |
| Strength Number | 2.5 |
| Strength Unit | mg/d |
| Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |
