JAIMIESS
These highlights do not include all the information needed to use safely and effectively. See full prescribing information for . Initial U.S. Approval: 1982
Approved
Approval ID
c094e6de-f1e9-9594-43f3-de1c1bb49bdb
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 25, 2024
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 and ethinyl estradiol and ethinyl estradiol tablets
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code70700-206
Application NumberANDA200492
Product Classification
M
Marketing Category
C73584
G
Generic Name
levonorgestrel and ethinyl estradiol and ethinyl estradiol tablets
Product Specifications
Effective DateNovember 25, 2024
FDA Product Classification