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EEMT
EEMT - 15310-020-01 - (ESTROGENS, ESTERIFIED and METHYLTESTOSTERONE)
Drug Information of EEMT
| Product NDC: | 15310-020 |
| Proprietary Name: | EEMT |
| Non Proprietary Name: | ESTROGENS, ESTERIFIED and METHYLTESTOSTERONE |
| Active Ingredient(s): | .625; 1.25 mg/1; mg/1 & nbsp; ESTROGENS, ESTERIFIED and METHYLTESTOSTERONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EEMT
| Product NDC: | 15310-020 |
| Labeler Name: | CREEKWOOD PHARMACEUTICAL, INC, |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110901 |
Package Information of EEMT
| Package NDC: | 15310-020-01 |
| Package Description: | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (15310-020-01) |
NDC Information of EEMT
| NDC Code | 15310-020-01 |
| Proprietary Name | EEMT |
| Package Description | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (15310-020-01) |
| Product NDC | 15310-020 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ESTROGENS, ESTERIFIED and METHYLTESTOSTERONE |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110901 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | CREEKWOOD PHARMACEUTICAL, INC, |
| Substance Name | ESTROGENS, ESTERIFIED; METHYLTESTOSTERONE |
| Strength Number | .625; 1.25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient] |
