NDC Package 71225-130-01 Merzee

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:
71225-130-01
Package Description:
1 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK
Product Code:
Proprietary Name:
Merzee
Non-Proprietary Name:
Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fumarate
Usage Information:
MERZEE is indicated for use by females of reproductive age to prevent pregnancy [see Clinical Studies (14)].The efficacy of MERZEE in women with a body mass index (BMI) of more than 35 kg/m2 has not been evaluated.
11-Digit NDC Billing Format:
71225013001
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1421459 - ethinyl estradiol 20 MCG / norethindrone acetate 1 MG Oral Capsule
  • RxCUI: 1421459 - ethinyl estradiol 0.02 MG / norethindrone acetate 1 MG Oral Capsule
  • RxCUI: 1421460 - ferrous fumarate 75 MG Oral Capsule
  • RxCUI: 1421461 - {24 (ethinyl estradiol 0.02 MG / norethindrone acetate 1 MG Oral Capsule) / 4 (ferrous fumarate 75 MG Oral Capsule) } Pack
  • RxCUI: 1421461 - Eth estra-Noreth Ac 0.02-1 MG (24) Oral Capsule / Ferr fum 75 MG (4) Oral Capsule 28 Day Pack
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Slayback Pharma Llc
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    ANDA212706
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-16-2021
    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 71225-130-01?

    The NDC Packaged Code 71225-130-01 is assigned to a package of 1 blister pack in 1 carton / 1 kit in 1 blister pack of Merzee, a human prescription drug labeled by Slayback Pharma Llc. The product's dosage form is kit and is administered via form.

    Is NDC 71225-130 included in the NDC Directory?

    Yes, Merzee with product code 71225-130 is active and included in the NDC Directory. The product was first marketed by Slayback Pharma Llc on February 16, 2021 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 NDC billing unit for package 71225-130-01?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

    What is the 11-digit format for NDC 71225-130-01?

    The 11-digit format is 71225013001. 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
    5-3-271225-130-015-4-271225-0130-01