CAMRESE - 0093-3134-82 - (levonorgestrel / ethinyl estradiol and ethinyl estradiol)

Alphabetical Index


Drug Information of CAMRESE

Product NDC: 0093-3134
Proprietary Name: CAMRESE
Non Proprietary Name: levonorgestrel / ethinyl estradiol and ethinyl estradiol
Active Ingredient(s):    & nbsp;   levonorgestrel / ethinyl estradiol and ethinyl estradiol
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of CAMRESE

Product NDC: 0093-3134
Labeler Name: TEVA Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021840
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20100728

Package Information of CAMRESE

Package NDC: 0093-3134-82
Package Description: 2 BLISTER PACK in 1 CARTON (0093-3134-82) > 1 KIT in 1 BLISTER PACK

NDC Information of CAMRESE

NDC Code 0093-3134-82
Proprietary Name CAMRESE
Package Description 2 BLISTER PACK in 1 CARTON (0093-3134-82) > 1 KIT in 1 BLISTER PACK
Product NDC 0093-3134
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levonorgestrel / ethinyl estradiol and ethinyl estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20100728
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name TEVA Pharmaceuticals USA Inc
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of CAMRESE


General Information