femhrt - 0430-0145-95 - (norethindrone acetate/ethinyl estradiol)

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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: 0430-0145-95
Package Description: 30 TRAY in 1 CASE (0430-0145-95) > 6 CARTON in 1 TRAY > 1 POUCH in 1 CARTON > 1 BLISTER PACK in 1 POUCH > 28 TABLET in 1 BLISTER PACK

NDC Information of femhrt

NDC Code 0430-0145-95
Proprietary Name femhrt
Package Description 30 TRAY in 1 CASE (0430-0145-95) > 6 CARTON in 1 TRAY > 1 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]

Complete Information of femhrt


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