APRI
Apri (desogestrel and ethinyl estradiol) Tablets
Approved
Approval ID
f3d91179-27e3-4bac-be47-8f224c836f5f
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 24, 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.
Desogestrel and Ethinyl Estradiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-4754
Application NumberANDA075256
Product Classification
M
Marketing Category
C73584
G
Generic Name
Desogestrel and Ethinyl Estradiol
Product Specifications
Effective DateApril 13, 2011
FDA Product Classification