Trivora
Revised: November 2007 IN-5427/S PHYSICIAN LABELING Trivora (levonorgestrel and ethinyl estradiol tablets USP) triphasic regimen Rx only
Approved
Approval ID
70d5c3f6-c7e4-4a6b-ad4f-2d3b9240c943
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 22, 2011
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.
Levonogestrel and Ethinyl Estradiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-4239
Application NumberANDA074538
Product Classification
M
Marketing Category
C73584
G
Generic Name
Levonogestrel and Ethinyl Estradiol
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 22, 2011
FDA Product Classification