NDC Package 60219-1031-7 Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fumarate

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

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:
60219-1031-7
Package Description:
3 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK (60219-1031-6)
Product Code:
Proprietary Name:
Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fumarate
Non-Proprietary Name:
Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fumarate
Usage Information:
Norethindrone acetate and ethinyl estradiol tablets and ferrous fumarate tablets are indicated for use by females of reproductive age 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 more than 35 kg/m2 has not been evaluated.
11-Digit NDC Billing Format:
60219103107
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.
    Sample Package:
    No
    FDA Application Number:
    ANDA207514
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-21-2017
    Listing Expiration Date:
    12-31-2024
    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 60219-1031-7?

    The NDC Packaged Code 60219-1031-7 is assigned to a package of 3 blister pack in 1 carton / 1 kit in 1 blister pack (60219-1031-6) of Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fumarate, a human prescription drug labeled by Amneal Pharmaceuticals Ny Llc. The product's dosage form is kit and is administered via form.

    Is NDC 60219-1031 included in the NDC Directory?

    Yes, Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fumarate with product code 60219-1031 is active and included in the NDC Directory. The product was first marketed by Amneal Pharmaceuticals Ny Llc on September 21, 2017 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 60219-1031-7?

    The 11-digit format is 60219103107. 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
    5-4-160219-1031-75-4-260219-1031-07