Nortrel - 0555-9009-57 - (Norethindrone and Ethinyl Estradiol)

Alphabetical Index


Drug Information of Nortrel

Product NDC: 0555-9009
Proprietary Name: Nortrel
Non Proprietary Name: Norethindrone and Ethinyl Estradiol
Active Ingredient(s): .035; 1    mg/1; mg/1 & nbsp;   Norethindrone and Ethinyl Estradiol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Nortrel

Product NDC: 0555-9009
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072693
Marketing Category: ANDA
Start Marketing Date: 20010613

Package Information of Nortrel

Package NDC: 0555-9009-57
Package Description: 6 BLISTER PACK in 1 CARTON (0555-9009-57) > 21 TABLET in 1 BLISTER PACK

NDC Information of Nortrel

NDC Code 0555-9009-57
Proprietary Name Nortrel
Package Description 6 BLISTER PACK in 1 CARTON (0555-9009-57) > 21 TABLET in 1 BLISTER PACK
Product NDC 0555-9009
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norethindrone and Ethinyl Estradiol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010613
Marketing Category Name ANDA
Labeler Name Barr Laboratories Inc.
Substance Name ETHINYL ESTRADIOL; NORETHINDRONE
Strength Number .035; 1
Strength Unit mg/1; mg/1
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA]

Complete Information of Nortrel


General Information