Kelnor 1/35
Kelnor™ 1/35 (28 Day Regimen)(ethynodiol diacetate and ethinyl estradiol tablets, USP)
Approved
Approval ID
994cefc2-0724-4b56-a816-ccdabef5492e
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.
ethynodiol diacetate and ethinyl estradiol
PRODUCT DETAILS
NDC Product Code54868-5942
Application NumberANDA076785
Marketing CategoryC73584
Route of AdministrationN/A
Effective DateApril 8, 2011
Generic Nameethynodiol diacetate and ethinyl estradiol