ENPRESSE
ENPRESSE™ – 28 TABLETS(levonorgestrel and ethinyl estradiol tablets, USP – triphasic regimen)
Approved
Approval ID
a3db80f8-5026-4954-aef5-dbf14c8c1b16
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 20, 2010
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.
levonorgestrel and ethinyl estradiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-4860
Application NumberANDA075809
Product Classification
M
Marketing Category
C73584
G
Generic Name
levonorgestrel and ethinyl estradiol
Product Specifications
Effective DateMarch 16, 2011
FDA Product Classification