Nortrel 7/7/7
(norethindrone and ethinyl estradiol tablets USP, 0.5/0.035 mg, 0.75/0.035 mg, and 1/0.035 mg)
Approved
Approval ID
992dcc56-90ab-4691-8114-16d47a8b9982
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 31, 2021
Manufacturers
FDA
Teva Pharmaceuticals USA, Inc.
DUNS: 001627975
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Norethindrone and Ethinyl Estradiol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0555-9012
Application NumberANDA075478
Product Classification
M
Marketing Category
C73584
G
Generic Name
Norethindrone and Ethinyl Estradiol
Product Specifications
Effective DateDecember 31, 2021
FDA Product Classification