Lutera - 54868-6210-0 - (Levonorgestrel and Ethinyl Estradiol)

Alphabetical Index


Drug Information of Lutera

Product NDC: 54868-6210
Proprietary Name: Lutera
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 Lutera

Product NDC: 54868-6210
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076625
Marketing Category: ANDA
Start Marketing Date: 20101213

Package Information of Lutera

Package NDC: 54868-6210-0
Package Description: 1 BLISTER PACK in 1 CARTON (54868-6210-0) > 1 KIT in 1 BLISTER PACK

NDC Information of Lutera

NDC Code 54868-6210-0
Proprietary Name Lutera
Package Description 1 BLISTER PACK in 1 CARTON (54868-6210-0) > 1 KIT in 1 BLISTER PACK
Product NDC 54868-6210
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levonorgestrel and Ethinyl Estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20101213
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Lutera


General Information