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femhrt
femhrt - 0430-0145-14 - (norethindrone acetate/ethinyl estradiol)
Drug Information of femhrt
| Product NDC: | 0430-0145 |
| Proprietary Name: | femhrt |
| Non Proprietary Name: | norethindrone acetate/ethinyl estradiol |
| Active Ingredient(s): | 2.5; .5 ug/1; mg/1 & nbsp; norethindrone acetate/ethinyl estradiol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of femhrt
| Product NDC: | 0430-0145 |
| Labeler Name: | Warner Chilcott (US), LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021065 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20091001 |
Package Information of femhrt
| Package NDC: | 0430-0145-14 |
| Package Description: | 72 CARTON in 1 CASE (0430-0145-14) > 5 POUCH in 1 CARTON > 1 BLISTER PACK in 1 POUCH > 28 TABLET in 1 BLISTER PACK |
NDC Information of femhrt
| NDC Code | 0430-0145-14 |
| Proprietary Name | femhrt |
| Package Description | 72 CARTON in 1 CASE (0430-0145-14) > 5 POUCH in 1 CARTON > 1 BLISTER PACK in 1 POUCH > 28 TABLET in 1 BLISTER PACK |
| Product NDC | 0430-0145 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norethindrone acetate/ethinyl estradiol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091001 |
| Marketing Category Name | NDA |
| Labeler Name | Warner Chilcott (US), LLC |
| Substance Name | ETHINYL ESTRADIOL; NORETHINDRONE ACETATE |
| Strength Number | 2.5; .5 |
| Strength Unit | ug/1; mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
