Enpresse - 21695-855-01 - (levonorgestrel and ethinyl estradiol)

Alphabetical Index


Drug Information of Enpresse

Product NDC: 21695-855
Proprietary Name: Enpresse
Non Proprietary Name: levonorgestrel and ethinyl estradiol
Active Ingredient(s):    & nbsp;   levonorgestrel and ethinyl estradiol
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Enpresse

Product NDC: 21695-855
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075809
Marketing Category: ANDA
Start Marketing Date: 20101220

Package Information of Enpresse

Package NDC: 21695-855-01
Package Description: 6 POUCH in 1 CARTON (21695-855-01) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK

NDC Information of Enpresse

NDC Code 21695-855-01
Proprietary Name Enpresse
Package Description 6 POUCH in 1 CARTON (21695-855-01) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK
Product NDC 21695-855
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levonorgestrel and ethinyl estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20101220
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Enpresse


General Information