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  5. NDC Package Code: 72275-725-77 Prilovixil

NDC Package 72275-725-77 Prilovixil

View Billable Units, 11-Digit Format, RxNorm

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 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:
72275-725-77
Package Description:
1 PACKAGE in 1 CARTON / 20 PACKAGE in 1 PACKAGE / 20 TUBE in 1 PACKAGE / 1 KIT in 1 TUBE * 30 g in 1 TUBE * 30 g in 1 TUBE * 30 g in 1 TUBE
Product Code:
72275-725
Proprietary Name:
Prilovixil
Usage Information:
Lidocaine and prilocaine cream (a eutectic mixture of lidocaine 2.5% and prilocaine 2.5%) is indicated as a topical anesthetic for use on: - normal intact skin for local analgesia. - genital mucous membranes for superficial minor surgery and as pretreatment for infiltration anesthesia. Lidocaine and prilocaine cream is not recommended in any clinical situation when penetration or migration beyond the tympanic membrane into the middle ear is possible because of the ototoxic effects observed in animal studies (see WARNINGS).
11-Digit NDC Billing Format:
72275072577
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 197877 - lidocaine 2.5 % / prilocaine 2.5 % Topical Cream
  • RxCUI: 197877 - lidocaine 25 MG/ML / prilocaine 25 MG/ML Topical Cream
    • Labeler Name:
    Primary Pharmaceuticals, Inc.
    Sample Package:
    No
    Start Marketing Date:
    11-09-2019
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    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 72275-725-77?

    The NDC Packaged Code 72275-725-77 is assigned to a package of 1 package in 1 carton / 20 package in 1 package / 20 tube in 1 package / 1 kit in 1 tube * 30 g in 1 tube * 30 g in 1 tube * 30 g in 1 tube of Prilovixil, labeled by Primary Pharmaceuticals, Inc.. The product's dosage form is and is administered via form.

    Is NDC 72275-725 included in the NDC Directory?

    No, Prilovixil with product code 72275-725 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Primary Pharmaceuticals, Inc. on November 09, 2019 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 72275-725-77?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units.

    What is the 11-digit format for NDC 72275-725-77?

    The 11-digit format is 72275072577. 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
    5-3-272275-725-775-4-272275-0725-77