Seasonale - 51285-058-66 - (levonorgestrel / ethinyl estradiol)

Alphabetical Index


Drug Information of Seasonale

Product NDC: 51285-058
Proprietary Name: Seasonale
Non Proprietary Name: levonorgestrel / ethinyl estradiol
Active Ingredient(s):    & nbsp;   levonorgestrel / ethinyl estradiol
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Seasonale

Product NDC: 51285-058
Labeler Name: Duramed Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021544
Marketing Category: NDA
Start Marketing Date: 20030509

Package Information of Seasonale

Package NDC: 51285-058-66
Package Description: 3 BLISTER PACK in 1 CARTON (51285-058-66) > 1 KIT in 1 BLISTER PACK

NDC Information of Seasonale

NDC Code 51285-058-66
Proprietary Name Seasonale
Package Description 3 BLISTER PACK in 1 CARTON (51285-058-66) > 1 KIT in 1 BLISTER PACK
Product NDC 51285-058
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levonorgestrel / ethinyl estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20030509
Marketing Category Name NDA
Labeler Name Duramed Pharmaceuticals, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Seasonale


General Information