OVCON 35 - 0430-0580-45 - (Norethindrone and Ethinyl Estradiol)

Alphabetical Index


Drug Information of OVCON 35

Product NDC: 0430-0580
Proprietary Name: OVCON 35
Non Proprietary Name: Norethindrone and Ethinyl Estradiol
Active Ingredient(s):    & nbsp;   Norethindrone and Ethinyl Estradiol
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of OVCON 35

Product NDC: 0430-0580
Labeler Name: Warner Chilcott (US), LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076238
Marketing Category: ANDA
Start Marketing Date: 20050601

Package Information of OVCON 35

Package NDC: 0430-0580-45
Package Description: 72 CARTON in 1 CASE (0430-0580-45) > 3 CELLO PACK in 1 CARTON > 1 BLISTER PACK in 1 CELLO PACK > 1 KIT in 1 BLISTER PACK

NDC Information of OVCON 35

NDC Code 0430-0580-45
Proprietary Name OVCON 35
Package Description 72 CARTON in 1 CASE (0430-0580-45) > 3 CELLO PACK in 1 CARTON > 1 BLISTER PACK in 1 CELLO PACK > 1 KIT in 1 BLISTER PACK
Product NDC 0430-0580
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norethindrone and Ethinyl Estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20050601
Marketing Category Name ANDA
Labeler Name Warner Chilcott (US), LLC
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of OVCON 35


General Information