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Estradiol / Norethindrone Acetate
Estradiol / Norethindrone Acetate - 54868-4677-0 - (Estradiol and Norethindrone Acetate)
Drug Information of Estradiol / Norethindrone Acetate
| Product NDC: | 54868-4677 |
| Proprietary Name: | Estradiol / Norethindrone Acetate |
| 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 Estradiol / Norethindrone Acetate
| Product NDC: | 54868-4677 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078324 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100310 |
Package Information of Estradiol / Norethindrone Acetate
| Package NDC: | 54868-4677-0 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (54868-4677-0) > 28 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Estradiol / Norethindrone Acetate
| NDC Code | 54868-4677-0 |
| Proprietary Name | Estradiol / Norethindrone Acetate |
| Package Description | 1 BLISTER PACK in 1 CARTON (54868-4677-0) > 28 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 54868-4677 |
| 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 | 20100310 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| 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] |
