NDC Package 70700-124-87 Lojaimiess

Levonorgestrel/ethinyl Estradiol And Ethinyl Estradiol 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:
70700-124-87
Package Description:
1 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK
Product Code:
Proprietary Name:
Lojaimiess
Non-Proprietary Name:
Levonorgestrel/ethinyl Estradiol And Ethinyl Estradiol
Usage Information:
Levonorgestrel and ethinyl estradiol tablets,and ethinyl estradiol tablets are indicated for use by women to prevent pregnancy.
11-Digit NDC Billing Format:
70700012487
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: 2117770 - {7 (ethinyl estradiol 0.01 MG Oral Tablet) / 84 (ethinyl estradiol 0.02 MG / levonorgestrel 0.1 MG Oral Tablet) } Pack [Lojaimiess 91 Day]
  • RxCUI: 2117770 - LoJaimiess 91 Day Pack
  • RxCUI: 2117770 - Lojaimiess 91 Day Pack
  • RxCUI: 242297 - levonorgestrel 0.1 MG / ethinyl estradiol 0.02 MG Oral Tablet
  • RxCUI: 242297 - ethinyl estradiol 0.02 MG / levonorgestrel 0.1 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Xiromed, Llc.
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    ANDA205131
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-11-2019
    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 70700-124-87?

    The NDC Packaged Code 70700-124-87 is assigned to a package of 1 blister pack in 1 carton / 1 kit in 1 blister pack of Lojaimiess, a human prescription drug labeled by Xiromed, Llc.. The product's dosage form is kit and is administered via form.

    Is NDC 70700-124 included in the NDC Directory?

    Yes, Lojaimiess with product code 70700-124 is active and included in the NDC Directory. The product was first marketed by Xiromed, Llc. on February 11, 2019 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 70700-124-87?

    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 70700-124-87?

    The 11-digit format is 70700012487. 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
    5-3-270700-124-875-4-270700-0124-87