Product NDC: | 54868-6272 |
Proprietary Name: | Junel 1.5/30 |
Non Proprietary Name: | norethindrone acetate and ethinyl estradiol |
Active Ingredient(s): | 30; 1.5 ug/1; mg/1 & nbsp; norethindrone acetate and ethinyl estradiol |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-6272 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076381 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110621 |
Package NDC: | 54868-6272-0 |
Package Description: | 1 BLISTER PACK in 1 CARTON (54868-6272-0) > 21 TABLET in 1 BLISTER PACK |
NDC Code | 54868-6272-0 |
Proprietary Name | Junel 1.5/30 |
Package Description | 1 BLISTER PACK in 1 CARTON (54868-6272-0) > 21 TABLET in 1 BLISTER PACK |
Product NDC | 54868-6272 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | norethindrone acetate and ethinyl estradiol |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110621 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE |
Strength Number | 30; 1.5 |
Strength Unit | ug/1; mg/1 |
Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |