Necon
Necon (Norethindrone and Ethinyl Estradiol Tablets, USP, 0.5 mg/0.035 mg)
Approved
Approval ID
1ca12bf6-9583-4578-8411-51ad02a405ec
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 23, 2024
Manufacturers
FDA
Dr. Reddy's Laboratories Inc.
DUNS: 802315887
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 Code75907-085
Application NumberANDA091204
Product Classification
M
Marketing Category
C73584
G
Generic Name
norethindrone and ethinyl estradiol
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 23, 2024
FDA Product Classification