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Testosterone - 44117-0001-1 - (Testosterone)
Drug Information of Testosterone
| Product NDC: | 44117-0001 |
| Proprietary Name: | Testosterone |
| Non Proprietary Name: | Testosterone |
| Active Ingredient(s): | 30 [hp_X]/mg & nbsp; Testosterone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Testosterone
| Product NDC: | 44117-0001 |
| Labeler Name: | Zoe Processing |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20130403 |
Package Information of Testosterone
| Package NDC: | 44117-0001-1 |
| Package Description: | 67600 mg in 1 BOTTLE (44117-0001-1) |
NDC Information of Testosterone
| NDC Code | 44117-0001-1 |
| Proprietary Name | Testosterone |
| Package Description | 67600 mg in 1 BOTTLE (44117-0001-1) |
| Product NDC | 44117-0001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Testosterone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130403 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Zoe Processing |
| Substance Name | TESTOSTERONE |
| Strength Number | 30 |
| Strength Unit | [hp_X]/mg |
| Pharmaceutical Classes |
