Portia
(levonorgestrel and ethinyl estradiol tablets USP)
Approved
Approval ID
c78b236b-85c4-4258-a524-cea08775100c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 12, 2025
Manufacturers
FDA
Teva Pharmaceuticals USA, Inc.
DUNS: 001627975
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
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0555-9020
Application NumberANDA075866
Product Classification
M
Marketing Category
C73584
G
Generic Name
Levonorgestrel and Ethinyl Estradiol
Product Specifications
Effective DateMarch 12, 2025
FDA Product Classification