Jinteli - 0093-3122-42 - (norethindrone acetate and ethinyl estradiol)

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Drug Information of Jinteli

Product NDC: 0093-3122
Proprietary Name: Jinteli
Non Proprietary Name: norethindrone acetate and ethinyl estradiol
Active Ingredient(s): 5; 1    ug/1; mg/1 & nbsp;   norethindrone acetate and ethinyl estradiol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Jinteli

Product NDC: 0093-3122
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076221
Marketing Category: ANDA
Start Marketing Date: 20110217

Package Information of Jinteli

Package NDC: 0093-3122-42
Package Description: 5 BLISTER PACK in 1 CARTON (0093-3122-42) > 28 TABLET in 1 BLISTER PACK (0093-3122-28)

NDC Information of Jinteli

NDC Code 0093-3122-42
Proprietary Name Jinteli
Package Description 5 BLISTER PACK in 1 CARTON (0093-3122-42) > 28 TABLET in 1 BLISTER PACK (0093-3122-28)
Product NDC 0093-3122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name norethindrone acetate and ethinyl estradiol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110217
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
Strength Number 5; 1
Strength Unit ug/1; mg/1
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA]

Complete Information of Jinteli


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