NDC Package 0264-9376-88 Lidocaine Hydrochloride

Injection Infiltration - View Billable Units, 11-Digit Format, RxNorm

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:
0264-9376-88
Package Description:
5 AMPULE in 1 CARTON / 5 mL in 1 AMPULE
Product Code:
Proprietary Name:
Lidocaine Hydrochloride
Non-Proprietary Name:
Lidocaine Hydrochloride
Substance Name:
Lidocaine Hydrochloride Anhydrous
Usage Information:
Lidocaine HCl Injection, USP is indicated for production of local or regional anesthesia by infiltration techniques such as percutaneous injection and intravenous regional anesthesia by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks, when the accepted procedures for these techniques as described in standard textbooks are observed.
11-Digit NDC Billing Format:
00264937688
NDC to RxNorm Crosswalk:
  • RxCUI: 1737566 - lidocaine HCl 1 % in 5 ML Injection
  • RxCUI: 1737566 - 5 ML lidocaine hydrochloride 10 MG/ML Injection
  • RxCUI: 1737566 - lidocaine HCl 1 % per 5 ML Injection
  • RxCUI: 1737566 - lidocaine HCl 50 MG per 5 ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    B. Braun Medical Inc.
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Infiltration - Administration that results in substances passing into tissue spaces or into cells.
  • Sample Package:
    No
    FDA Application Number:
    ANDA208474
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-03-2018
    Listing Expiration Date:
    12-31-2024
    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 0264-9376-88?

    The NDC Packaged Code 0264-9376-88 is assigned to a package of 5 ampule in 1 carton / 5 ml in 1 ampule of Lidocaine Hydrochloride, a human prescription drug labeled by B. Braun Medical Inc.. The product's dosage form is injection and is administered via infiltration form.

    Is NDC 0264-9376 included in the NDC Directory?

    Yes, Lidocaine Hydrochloride with product code 0264-9376 is active and included in the NDC Directory. The product was first marketed by B. Braun Medical Inc. on August 03, 2018 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0264-9376-88?

    The 11-digit format is 00264937688. 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 4-4-2 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
    4-4-20264-9376-885-4-200264-9376-88