JAIMIESS
These highlights do not include all the information needed to use JAIMIESS safely and effectively. See full prescribing information for JAIMIESS. Initial U.S. Approval: 1982
Approved
Approval ID
7fe3a0d4-533f-0bdf-e60a-20c69bdf79fc
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 21, 2023
Manufacturers
FDA
Xiromed, LLC.
DUNS: 080228637
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
NDC Product Code70700-123
Application NumberANDA203770
Marketing CategoryC73584
Route of AdministrationN/A
Effective DateJanuary 1, 2018
Generic Namelevonorgestrel / ethinyl estradiol and ethinyl estradiol