NDC Package 79929-005-07 Norethindrone And Ethinyl Estradiol And Ferrous Fumarate

Norethindrone And Ethinyl Estradiol And Ferrous Fumarate Tablet 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:
79929-005-07
Package Description:
3 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK
Product Code:
Proprietary Name:
Norethindrone And Ethinyl Estradiol And Ferrous Fumarate
Non-Proprietary Name:
Norethindrone And Ethinyl Estradiol And Ferrous Fumarate Tablet
Usage Information:
Norethindrone and ethinyl estradiol tablets (chewable) 0.4 mg/0.035 mg and ferrous fumarate tablets are indicated for use by females of reproductive potential to prevent pregnancy.
11-Digit NDC Billing Format:
79929000507
NDC to RxNorm Crosswalk:
  • RxCUI: 1095223 - ferrous fumarate 75 MG Chewable Tablet
  • RxCUI: 1095224 - {21 (ethinyl estradiol 0.035 MG / norethindrone 0.4 MG Chewable Tablet) / 7 (ferrous fumarate 75 MG Chewable Tablet) } Pack
  • RxCUI: 1095224 - eth-estra-noreth 0.035-0.4 MG (21) Chewable Tablet / ferr fum 75 MG (7) Chewable Tablet 28 Day Pack
  • RxCUI: 1095224 - {21 (ethinyl estradiol 35 MCG / norethindrone 0.4 MG Chewable Tablet) / 7 (ferrous fumarate 75 MG Chewable Tablet) } Pack
  • RxCUI: 433718 - norethindrone 0.4 MG / ethinyl estradiol 35 MCG Chewable Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Naari Pte Limited
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    ANDA207066
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-31-2022
    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 79929-005-07?

    The NDC Packaged Code 79929-005-07 is assigned to a package of 3 blister pack in 1 carton / 1 kit in 1 blister pack of Norethindrone And Ethinyl Estradiol And Ferrous Fumarate, a human prescription drug labeled by Naari Pte Limited. The product's dosage form is kit and is administered via form.

    Is NDC 79929-005 included in the NDC Directory?

    Yes, Norethindrone And Ethinyl Estradiol And Ferrous Fumarate with product code 79929-005 is active and included in the NDC Directory. The product was first marketed by Naari Pte Limited on December 31, 2022 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 79929-005-07?

    The 11-digit format is 79929000507. 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 5-3-2 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
    5-3-279929-005-075-4-279929-0005-07