Trivora
Trivora-28 (levonorgestrel and ethinyl estradiol tablets USP) triphasic regimen
Approved
Approval ID
45293c33-9f32-46c8-a8ec-07a0fb8b7c4f
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 3, 2022
Manufacturers
FDA
Mayne Pharma Inc.
DUNS: 867220261
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 Code51862-510
Application NumberANDA074538
Product Classification
M
Marketing Category
C73584
G
Generic Name
Levonorgestrel and Ethinyl Estradiol
Product Specifications
Effective DateMarch 3, 2022
FDA Product Classification