NDC Package 75907-088-13 Haloette

View Billable Units, 11-Digit Format, RxNorm

Package Information
Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:

75907-088-13

Package Description:

3 POUCH in 1 CARTON / 21 d in 1 POUCH (75907-088-11)

Product Code:

75907-088

Proprietary Name:

Haloette

Usage Information:

FOR VAGINAL USE ONLYHaloette® is indicated for use by females of reproductive age to prevent pregnancy.

11-Digit NDC Billing Format:

75907008813

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: 1367436 - etonogestrel 0.12 MG / ethinyl estradiol 0.015 MG per 24HR 3 Week Vaginal System
RxCUI: 1367436 - 21 DAY ethinyl estradiol 0.000625 MG/HR / etonogestrel 0.005 MG/HR Vaginal System
RxCUI: 1367436 - ethinyl estradiol 0.015 MG / etonogestrel 0.12 MG per 24HR 3 Week Vaginal System
RxCUI: 1367436 - ethinyl estradiol 15 MCG / etonogestrel 120 MCG per 24HR 3 Week Vaginal System
RxCUI: 2622921 - HALOETTE 0.12 MG / 0.015 MG per 24HR 3 Week Vaginal System

Labeler Name:

Dr. Reddy's Labratories Inc.

Sample Package:

FDA Application Number:

ANDA211328

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

05-28-2024

Listing Expiration Date:

12-31-2025

Exclude Flag:

Code Structure:

75907 - Dr. Reddy's Labratories Inc.
- 75907-088 - Haloette
  - 75907-088-13 - 3 POUCH in 1 CARTON / 21 d in 1 POUCH (75907-088-11)

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 75907-088-13?

The NDC Packaged Code 75907-088-13 is assigned to a package of 3 pouch in 1 carton / 21 d in 1 pouch (75907-088-11) of Haloette, labeled by Dr. Reddy's Labratories Inc.. The product's dosage form is and is administered via form.

Is NDC 75907-088 included in the NDC Directory?

No, Haloette with product code 75907-088 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Dr. Reddy's Labratories Inc. on May 28, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 75907-088-13?

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 75907-088-13?

The 11-digit format is 75907008813. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	75907-088-13	5-4-2	75907-0088-13

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