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ESTRADIOL
ESTRADIOL - 16590-278-30 - (ESTRADIOL)
Drug Information of ESTRADIOL
| Product NDC: | 16590-278 |
| Proprietary Name: | ESTRADIOL |
| 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 ESTRADIOL
| Product NDC: | 16590-278 |
| Labeler Name: | STAT Rx USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040114 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960314 |
Package Information of ESTRADIOL
| Package NDC: | 16590-278-30 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (16590-278-30) |
NDC Information of ESTRADIOL
| NDC Code | 16590-278-30 |
| Proprietary Name | ESTRADIOL |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (16590-278-30) |
| Product NDC | 16590-278 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ESTRADIOL |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19960314 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT Rx USA LLC |
| Substance Name | ESTRADIOL |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
