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  5. NDC Package Code: 70700-152-85 Gemmily

NDC Package 70700-152-85 Gemmily

Norethindrone Acetate And Ethinyl Estradiol,And Ferrous Fumarate Kit - 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:
70700-152-85
Package Description:
3 CARTON in 1 CARTON / 1 BLISTER PACK in 1 CARTON (70700-152-84) / 1 KIT in 1 BLISTER PACK
Product Code:
70700-152
Proprietary Name:
Gemmily
Non-Proprietary Name:
Norethindrone Acetate And Ethinyl Estradiol, And Ferrous Fumarate
Usage Information:
Gemmily is indicated for use by females of reproductive age to prevent pregnancy [see Clinical Studies (14)]. The efficacy of Gemmily in women with a body mass index (BMI) of more than 35 kg/m2 has not been evaluated.
11-Digit NDC Billing Format:
70700015285
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:
    Xiromed, Llc
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    ANDA213317
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-09-2020
    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 70700-152-85?

    The NDC Packaged Code 70700-152-85 is assigned to a package of 3 carton in 1 carton / 1 blister pack in 1 carton (70700-152-84) / 1 kit in 1 blister pack of Gemmily, a human prescription drug labeled by Xiromed, Llc. The product's dosage form is kit and is administered via form.

    Is NDC 70700-152 included in the NDC Directory?

    Yes, Gemmily with product code 70700-152 is active and included in the NDC Directory. The product was first marketed by Xiromed, Llc on November 09, 2020 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 70700-152-85?

    The 11-digit format is 70700015285. 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
    5-3-270700-152-855-4-270700-0152-85