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Activella
Activella - 0169-5174-02 - (estradiol and norethindrone acetate)
Drug Information of Activella
| Product NDC: | 0169-5174 |
| Proprietary Name: | Activella |
| Non Proprietary Name: | estradiol and norethindrone acetate |
| Active Ingredient(s): | 1; .5 mg/1; mg/1 & nbsp; estradiol and norethindrone acetate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Activella
| Product NDC: | 0169-5174 |
| Labeler Name: | Novo Nordisk |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020907 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030722 |
Package Information of Activella
| Package NDC: | 0169-5174-02 |
| Package Description: | 1 DIALPACK in 1 CARTON (0169-5174-02) > 28 TABLET, FILM COATED in 1 DIALPACK |
NDC Information of Activella
| NDC Code | 0169-5174-02 |
| Proprietary Name | Activella |
| Package Description | 1 DIALPACK in 1 CARTON (0169-5174-02) > 28 TABLET, FILM COATED in 1 DIALPACK |
| Product NDC | 0169-5174 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | estradiol and norethindrone acetate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20030722 |
| Marketing Category Name | NDA |
| Labeler Name | Novo Nordisk |
| Substance Name | ESTRADIOL; NORETHINDRONE ACETATE |
| Strength Number | 1; .5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
