Enpresse
ENPRESSE™ – 28 TABLETS(levonorgestrel and ethinyl estradiol tablets, USP – triphasic regimen)
Approved
Approval ID
6c095eec-8d92-4b07-8f9e-84bb8c9bc3f8
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 26, 2011
Manufacturers
FDA
Rebel Distributors Corp
DUNS: 118802834
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 Code21695-855
Application NumberANDA075809
Product Classification
M
Marketing Category
C73584
G
Generic Name
levonorgestrel and ethinyl estradiol
Product Specifications
Effective DateDecember 20, 2010
FDA Product Classification