Emergency Contraceptive
NDC Package 59726-138-01

11-digit billing NDC: 59726013801
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Emergency Contraceptive is take as soon as possible within 72 hours (3 days) after unprotected sex. Marketed by P & L Development, Llc, this product is identified by NDC 59726-138 and is authorized under FDA application ANDA205329.

Identification & Billing

NDC Package Code
59726-138-01
Package Description
1 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK
Product Code
59726-138
11-Digit Billing Format
59726013801

Clinical Specifications

Proprietary Name
Emergency Contraceptive
Dosage Form
-
Usage Information
Take as soon as possible within 72 hours (3 days) after unprotected sex. The sooner you take it the better it will work.if you vomit within 2 hours after taking the medication, call a healthcare professional to find out if you should repeat the dose.

Regulatory & Marketing

Labeler Name
P & L Development, Llc
FDA Application #
ANDA205329
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
08-01-2023
End Marketing Date
09-01-2026
Listing Expiration
09-01-2026
Exclude Flag
D
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 59726-138-01 identifies a specific commercial package of 1 blister pack in 1 carton / 1 tablet in 1 blister pack of Emergency Contraceptive, labeled by P & L Development, Llc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by P & L Development, Llc on August 01, 2023. The current certification is valid through September 01, 2026.

How is this P & L Development, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 59726013801. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
59726-138-01
11-Digit CMS (5-4-2)
59726-0138-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.