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  5. NDC Package Code: 70700-206-93 Jaimiess

NDC Package 70700-206-93 Jaimiess

Levonorgestrel And Ethinyl Estradiol And Ethinyl Estradiol Tablets 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:
70700-206-93
Package Description:
2 POUCH in 1 CARTON / 1 BLISTER PACK in 1 POUCH (70700-206-87) / 1 KIT in 1 BLISTER PACK
Product Code:
70700-206
Proprietary Name:
Jaimiess
Non-Proprietary Name:
Levonorgestrel And Ethinyl Estradiol And Ethinyl Estradiol Tablets
Usage Information:
Jaimiess is indicated for use by females of reproductive potential to prevent pregnancy.
11-Digit NDC Billing Format:
70700020693
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
2 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 2001751 - {7 (ethinyl estradiol 0.01 MG Oral Tablet) / 84 (ethinyl estradiol 0.03 MG / levonorgestrel 0.15 MG Oral Tablet) } Pack [Jaimiess 91 Day]
  • RxCUI: 2001751 - Jaimiess 91 Day Pack
  • RxCUI: 238019 - levonorgestrel 0.15 MG / ethinyl estradiol 0.03 MG Oral Tablet
  • RxCUI: 238019 - ethinyl estradiol 0.03 MG / levonorgestrel 0.15 MG Oral Tablet
  • RxCUI: 248310 - ethinyl estradiol 0.01 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:
ANDA200492
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
01-29-2025
Listing Expiration Date:
12-31-2026
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 70700-206-93?

The NDC Packaged Code 70700-206-93 is assigned to a package of 2 pouch in 1 carton / 1 blister pack in 1 pouch (70700-206-87) / 1 kit in 1 blister pack of Jaimiess, a human prescription drug labeled by Xiromed Llc. The product's dosage form is kit and is administered via form.

Is NDC 70700-206 included in the NDC Directory?

Yes, Jaimiess with product code 70700-206 is active and included in the NDC Directory. The product was first marketed by Xiromed Llc on January 29, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 70700-206-93?

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 2.

What is the 11-digit format for NDC 70700-206-93?

The 11-digit format is 70700020693. 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
5-3-270700-206-935-4-270700-0206-93