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Estrace
Estrace - 54868-0494-1 - (estradiol)
Drug Information of Estrace
| Product NDC: | 54868-0494 |
| Proprietary Name: | Estrace |
| Non Proprietary Name: | estradiol |
| Active Ingredient(s): | 1 mg/1 & nbsp; estradiol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Estrace
| Product NDC: | 54868-0494 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA084499 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960416 |
Package Information of Estrace
| Package NDC: | 54868-0494-1 |
| Package Description: | 30 TABLET in 1 BOTTLE (54868-0494-1) |
NDC Information of Estrace
| NDC Code | 54868-0494-1 |
| Proprietary Name | Estrace |
| Package Description | 30 TABLET in 1 BOTTLE (54868-0494-1) |
| Product NDC | 54868-0494 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | estradiol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19960416 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | ESTRADIOL |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
