Jolessa - 0555-9123-66 - (levonorgestrel / ethinyl estradiol)

Alphabetical Index


Drug Information of Jolessa

Product NDC: 0555-9123
Proprietary Name: Jolessa
Non Proprietary Name: levonorgestrel / ethinyl estradiol
Active Ingredient(s):    & nbsp;   levonorgestrel / ethinyl estradiol
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Jolessa

Product NDC: 0555-9123
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021544
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20031013

Package Information of Jolessa

Package NDC: 0555-9123-66
Package Description: 3 BLISTER PACK in 1 CARTON (0555-9123-66) > 1 KIT in 1 BLISTER PACK

NDC Information of Jolessa

NDC Code 0555-9123-66
Proprietary Name Jolessa
Package Description 3 BLISTER PACK in 1 CARTON (0555-9123-66) > 1 KIT in 1 BLISTER PACK
Product NDC 0555-9123
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levonorgestrel / ethinyl estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20031013
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Barr Laboratories Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Jolessa


General Information