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LoSeasonique - 54868-6275-0 - (levonorgestrel/ethinyl estradiol and ethinyl estradiol)

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Drug Information of LoSeasonique

Product NDC: 54868-6275
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: 54868-6275
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022262
Marketing Category: NDA
Start Marketing Date: 20110621

Package Information of LoSeasonique

Package NDC: 54868-6275-0
Package Description: 1 BLISTER PACK in 1 BOX (54868-6275-0) > 1 KIT in 1 BLISTER PACK

NDC Information of LoSeasonique

NDC Code 54868-6275-0
Proprietary Name LoSeasonique
Package Description 1 BLISTER PACK in 1 BOX (54868-6275-0) > 1 KIT in 1 BLISTER PACK
Product NDC 54868-6275
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levonorgestrel/ethinyl estradiol and ethinyl estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20110621
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of LoSeasonique


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