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Esterified Estrogens and Methyltestosterone
Esterified Estrogens and Methyltestosterone - 50220-001-01 - (Esterified Estrogens and Methyltestosterone)
Drug Information of Esterified Estrogens and Methyltestosterone
| Product NDC: | 50220-001 |
| Proprietary Name: | Esterified Estrogens and Methyltestosterone |
| Non Proprietary Name: | Esterified Estrogens and Methyltestosterone |
| Active Ingredient(s): | .625; 1.25 mg/1; mg/1 & nbsp; Esterified Estrogens and Methyltestosterone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Esterified Estrogens and Methyltestosterone
| Product NDC: | 50220-001 |
| Labeler Name: | Tal Pharma LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100917 |
Package Information of Esterified Estrogens and Methyltestosterone
| Package NDC: | 50220-001-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (50220-001-01) |
NDC Information of Esterified Estrogens and Methyltestosterone
| NDC Code | 50220-001-01 |
| Proprietary Name | Esterified Estrogens and Methyltestosterone |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (50220-001-01) |
| Product NDC | 50220-001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Esterified Estrogens and Methyltestosterone |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100917 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Tal Pharma LLC |
| Substance Name | ESTRONE SODIUM SULFATE; METHYLTESTOSTERONE |
| Strength Number | .625; 1.25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |
