Zovia 1/35E-28
(Ethynodiol Diacetate and Ethinyl Estradiol Tablets USP)Revised: August 2006Rx only
Approved
Approval ID
e7d7b18e-101a-49ab-bf6c-c57a5abbe815
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 13, 2012
Manufacturers
FDA
Physicians Total Care, Inc.
DUNS: 194123980
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ethynodiol Diacetate and Ethinyl Estradiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-4240
Application NumberANDA072721
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ethynodiol Diacetate and Ethinyl Estradiol
Product Specifications
Route of AdministrationORAL
Effective DateApril 13, 2012
FDA Product Classification
Ethynodiol Diacetate and Ethinyl Estradiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-4778
Application NumberANDA072723
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ethynodiol Diacetate and Ethinyl Estradiol
Product Specifications
Route of AdministrationORAL
Effective DateApril 13, 2012
FDA Product Classification