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METHITEST
METHITEST - 0115-7037-01 - (METHYLTESTOSTERONE)
Drug Information of METHITEST
| Product NDC: | 0115-7037 |
| Proprietary Name: | METHITEST |
| Non Proprietary Name: | METHYLTESTOSTERONE |
| Active Ingredient(s): | 10 mg/1 & nbsp; METHYLTESTOSTERONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of METHITEST
| Product NDC: | 0115-7037 |
| Labeler Name: | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080767 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19741017 |
Package Information of METHITEST
| Package NDC: | 0115-7037-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0115-7037-01) |
NDC Information of METHITEST
| NDC Code | 0115-7037-01 |
| Proprietary Name | METHITEST |
| Package Description | 100 TABLET in 1 BOTTLE (0115-7037-01) |
| Product NDC | 0115-7037 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METHYLTESTOSTERONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19741017 |
| Marketing Category Name | ANDA |
| Labeler Name | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
| Substance Name | METHYLTESTOSTERONE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |
