CRYSELLE
CRYSELLE™ - 28 TABLETS(NORGESTREL AND ETHINYL ESTRADIOL TABLETS, USP)
Approved
Approval ID
cf19bbd6-91d1-4cbd-9fc4-5c750451f666
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 20, 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.
norgestrel and ethinyl estradiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-4851
Application NumberANDA075840
Product Classification
M
Marketing Category
C73584
G
Generic Name
norgestrel and ethinyl estradiol
Product Specifications
Effective DateApril 8, 2011
FDA Product Classification