Jencycla - 68180-877-13 - (norethindrone)

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Drug Information of Jencycla

Product NDC: 68180-877
Proprietary Name: Jencycla
Non Proprietary Name: norethindrone
Active Ingredient(s): .35    mg/1 & nbsp;   norethindrone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Jencycla

Product NDC: 68180-877
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091323
Marketing Category: ANDA
Start Marketing Date: 20130508

Package Information of Jencycla

Package NDC: 68180-877-13
Package Description: 1 BLISTER PACK in 1 CARTON (68180-877-13) > 28 TABLET in 1 BLISTER PACK (68180-877-11)

NDC Information of Jencycla

NDC Code 68180-877-13
Proprietary Name Jencycla
Package Description 1 BLISTER PACK in 1 CARTON (68180-877-13) > 28 TABLET in 1 BLISTER PACK (68180-877-11)
Product NDC 68180-877
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name norethindrone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130508
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, Inc.
Substance Name NORETHINDRONE
Strength Number .35
Strength Unit mg/1
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Jencycla


General Information