MedPath

Necon

Necon 1/35 (Norethindrone and Ethinyl Estradiol Tablets USP) Rx only

Approved
Approval ID

2de68f9e-fa13-4b87-84f9-dbb73883ba40

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Mar 15, 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.

Norethindrone and Ethinyl Estradiol

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code21695-857
Application NumberANDA070687
Product Classification
M
Marketing Category
C73584
G
Generic Name
Norethindrone and Ethinyl Estradiol
Product Specifications
Effective DateMarch 15, 2011
FDA Product Classification

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Necon - FDA Drug Approval Details