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  5. NDC Package Code: 69238-1582-3 Norethindrone Acetate And Ethinyl Estradiol

NDC Package 69238-1582-3 Norethindrone Acetate And Ethinyl Estradiol

Kit Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
69238-1582-3
Package Description:
3 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK (69238-1582-9)
Product Code:
69238-1582
Proprietary Name:
Norethindrone Acetate And Ethinyl Estradiol
Non-Proprietary Name:
Norethindrone Acetate And Ethinyl Estradiol
Usage Information:
Norethindrone acetate and ethinyl estradiol tablets and ferrous fumarate tablets are indicated for use by women to prevent pregnancy [see Clinical Studies (14)]. The efficacy of norethindrone acetate and ethinyl estradiol tablets and ferrous fumarate tablets in women with a body mass index (BMI) of > 35 kg/m2 has not been evaluated.
11-Digit NDC Billing Format:
69238158203
NDC to RxNorm Crosswalk:
  • RxCUI: 1358762 - norethindrone acetate 1 MG / ethinyl estradiol 0.02 MG Oral Tablet
  • RxCUI: 1358762 - ethinyl estradiol 0.02 MG / norethindrone acetate 1 MG Oral Tablet
  • RxCUI: 1358762 - ethinyl estradiol 20 MCG / norethindrone acetate 1 MG Oral Tablet
  • RxCUI: 1359117 - {24 (ethinyl estradiol 0.02 MG / norethindrone acetate 1 MG Oral Tablet) / 4 (ferrous fumarate 75 MG Oral Tablet) } Pack
  • RxCUI: 1359117 - Eth estra-Noreth Ac 0.02-1 MG (24) Oral Tablet / Ferr fum 75 MG (4) Oral Tablet 28 Day Pack
Product Type:
Human Prescription Drug
Labeler Name:
Amneal Pharmaceuticals Ny Llc
Dosage Form:
Kit - A packaged collection of related material.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Sample Package:
No
FDA Application Number:
ANDA078267
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
12-20-2013
Listing Expiration Date:
12-31-2025
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 69238-1582-3?

The NDC Packaged Code 69238-1582-3 is assigned to a package of 3 blister pack in 1 carton / 1 kit in 1 blister pack (69238-1582-9) of Norethindrone Acetate And Ethinyl Estradiol, a human prescription drug labeled by Amneal Pharmaceuticals Ny Llc. The product's dosage form is kit and is administered via oral form.

Is NDC 69238-1582 included in the NDC Directory?

Yes, Norethindrone Acetate And Ethinyl Estradiol with product code 69238-1582 is active and included in the NDC Directory. The product was first marketed by Amneal Pharmaceuticals Ny Llc on December 20, 2013 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 69238-1582-3?

The 11-digit format is 69238158203. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-169238-1582-35-4-269238-1582-03