Amethia - 52544-268-29 - (levonorgestrel and ethinyl estradiol and ethinyl estradiol)

Alphabetical Index


Drug Information of Amethia

Product NDC: 52544-268
Proprietary Name: Amethia
Non Proprietary Name: levonorgestrel and ethinyl estradiol and ethinyl estradiol
Active Ingredient(s):    & nbsp;   levonorgestrel and ethinyl estradiol and ethinyl estradiol
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Amethia

Product NDC: 52544-268
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078834
Marketing Category: ANDA
Start Marketing Date: 20110531

Package Information of Amethia

Package NDC: 52544-268-29
Package Description: 2 BLISTER PACK in 1 CARTON (52544-268-29) > 1 KIT in 1 BLISTER PACK (52544-268-84)

NDC Information of Amethia

NDC Code 52544-268-29
Proprietary Name Amethia
Package Description 2 BLISTER PACK in 1 CARTON (52544-268-29) > 1 KIT in 1 BLISTER PACK (52544-268-84)
Product NDC 52544-268
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levonorgestrel and ethinyl estradiol and ethinyl estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20110531
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Amethia


General Information