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LoSeasonique - 51285-092-87 - (levonorgestrel/ethinyl estradiol and ethinyl estradiol)

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Drug Information of LoSeasonique

Product NDC: 51285-092
Proprietary Name: LoSeasonique
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 LoSeasonique

Product NDC: 51285-092
Labeler Name: Teva Women's Health, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022262
Marketing Category: NDA
Start Marketing Date: 20081024

Package Information of LoSeasonique

Package NDC: 51285-092-87
Package Description: 2 BLISTER PACK in 1 BOX (51285-092-87) > 1 KIT in 1 BLISTER PACK

NDC Information of LoSeasonique

NDC Code 51285-092-87
Proprietary Name LoSeasonique
Package Description 2 BLISTER PACK in 1 BOX (51285-092-87) > 1 KIT in 1 BLISTER PACK
Product NDC 51285-092
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levonorgestrel/ethinyl estradiol and ethinyl estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20081024
Marketing Category Name NDA
Labeler Name Teva Women's Health, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of LoSeasonique


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