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  5. NDC Package Code: 50090-3122-0 Junel Fe 28 Day

NDC Package 50090-3122-0 Junel Fe 28 Day

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:
50090-3122-0
Package Description:
6 POUCH in 1 CARTON / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACK
Product Code:
50090-3122
Proprietary Name:
Junel Fe 28 Day
Non-Proprietary Name:
Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fumarate
Usage Information:
Junel 21 and Junel Fe 28 are indicated for the prevention of pregnancy in women who elect to use oral contraceptives as a method of contraception.Oral contraceptives are highly effective. Table I lists the typical accidental pregnancy rates for users of combination oral contraceptives and other methods of contraception. The efficacy of these contraceptive methods, except sterilization, depends upon the reliability with which they are used. Correct and consistent use of methods can result in lower failure rates.TABLE I: LOWEST EXPECTED AND TYPICAL FAILURE RATES DURING THE FIRST YEAR OF CONTINUOUS USE OF A METHOD% Of Women Experiencing an Unintended Pregnancy in the First Year of Continuous UseMethodLowest Expected*Typical**(No contraception)(85)(85)Oral contraceptives combined progestin only 0.1 0.53 N/A*** N/A***Diaphragm with spermicidal cream or jelly620Spermicides alone (foam, creams, gels, vaginal suppositories, and vaginal film)626Vaginal Sponge nulliparous parous 9 20 20 40Implant0.050.05Injection: depot medroxyprogesterone acetate0.30.3IUD progesterone T copper T 380A LNg 20 1.5 0.6 0.1 2 0.8 0.1Condom without spermicides female male 5 3 21 14Cervical Cap with spermicidal cream or jelly nulliparous parous9 2620 40Periodic abstinence (all methods)1 to 925Withdrawal419Female sterilization0.50.5Male sterilization0.100.15Adapted from RA Hatcher et al, Reference 7.* The authors' best guess of the percentage of women expected to experience an accidental pregnancy among couples who initiate a method (not necessarily for the first time)     and who use it consistently and correctly during the first year if they do not stop for any other reason. ** This term represents “typical” couples who initiate use of a method (not necessarily for the first time), who experience an accidental pregnancy during the first year if they do      not stop use for any other reason.*** N/A-Data not available.
11-Digit NDC Billing Format:
50090312200
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
6 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1359022 - norethindrone acetate 1.5 MG / ethinyl estradiol 30 MCG Oral Tablet
  • RxCUI: 1359022 - ethinyl estradiol 0.03 MG / norethindrone acetate 1.5 MG Oral Tablet
  • RxCUI: 1359022 - ethinyl estradiol 30 MCG / norethindrone acetate 1.5 MG Oral Tablet
  • RxCUI: 1359023 - {21 (ethinyl estradiol 0.03 MG / norethindrone acetate 1.5 MG Oral Tablet) / 7 (ferrous fumarate 75 MG Oral Tablet) } Pack
  • RxCUI: 1359023 - Eth estra-Noreth Ac 0.03-1.5 MG (21) Oral Tablet / Ferr fum 75 MG (7) Oral Tablet 28 Day Pack
Product Type:
Human Prescription Drug
Labeler Name:
A-s Medication Solutions
Dosage Form:
Kit - A packaged collection of related material.
Sample Package:
No
FDA Application Number:
ANDA076064
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
09-18-2003
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 50090-3122-0?

The NDC Packaged Code 50090-3122-0 is assigned to a package of 6 pouch in 1 carton / 1 blister pack in 1 pouch / 1 kit in 1 blister pack of Junel Fe 28 Day, a human prescription drug labeled by A-s Medication Solutions. The product's dosage form is kit and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 6 billable units per package.

Is NDC 50090-3122 included in the NDC Directory?

Yes, Junel Fe 28 Day with product code 50090-3122 is active and included in the NDC Directory. The product was first marketed by A-s Medication Solutions on September 18, 2003 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 50090-3122-0?

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 6.

What is the 11-digit format for NDC 50090-3122-0?

The 11-digit format is 50090312200. 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 5-4-1 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
5-4-150090-3122-05-4-250090-3122-00