LoSeasonique
These highlights do not include all the information needed to use LoSeasonique tablets safely and effectively. See full prescribing information for LoSeasonique.LoSeasonique (levonorgestrel/ethinyl estradiol tablets and ethinyl estradiol tablets) for oral useInitial U.S. Approval: 1982
Approved
Approval ID
676f6a52-8d82-4289-ae35-28eb4fbbc184
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 10, 2012
Manufacturers
FDA
Physicians Total Care, Inc.
DUNS: 194123980
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
levonorgestrel/ethinyl estradiol and ethinyl estradiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-6275
Application NumberNDA022262
Product Classification
M
Marketing Category
C73594
G
Generic Name
levonorgestrel/ethinyl estradiol and ethinyl estradiol
Product Specifications
Effective DateJanuary 10, 2012
FDA Product Classification