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CombiPatch
CombiPatch - 0078-0377-42 - (estradiol and norethindrone acetate)
Drug Information of CombiPatch
| Product NDC: | 0078-0377 |
| Proprietary Name: | CombiPatch |
| Non Proprietary Name: | estradiol and norethindrone acetate |
| Active Ingredient(s): | .05; .14 mg/d; mg/d & nbsp; estradiol and norethindrone acetate |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CombiPatch
| Product NDC: | 0078-0377 |
| Labeler Name: | Novartis Pharmaceuticals Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020870 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19980807 |
Package Information of CombiPatch
| Package NDC: | 0078-0377-42 |
| Package Description: | 8 PATCH in 1 CARTON (0078-0377-42) > 3.5 d in 1 PATCH |
NDC Information of CombiPatch
| NDC Code | 0078-0377-42 |
| Proprietary Name | CombiPatch |
| Package Description | 8 PATCH in 1 CARTON (0078-0377-42) > 3.5 d in 1 PATCH |
| Product NDC | 0078-0377 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | estradiol and norethindrone acetate |
| Dosage Form Name | PATCH, EXTENDED RELEASE |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 19980807 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Pharmaceuticals Corporation |
| Substance Name | ESTRADIOL; NORETHINDRONE ACETATE |
| Strength Number | .05; .14 |
| Strength Unit | mg/d; mg/d |
| Pharmaceutical Classes | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
