NDC Package 13533-618-10 Hyperrab S/d

Rabies Immune Globulin (human) Injection Intramuscular - 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:
13533-618-10
Package Description:
1 VIAL in 1 CARTON / 10 mL in 1 VIAL (13533-618-11)
Product Code:
Proprietary Name:
Hyperrab S/d
Non-Proprietary Name:
Rabies Immune Globulin (human)
Substance Name:
Human Rabies Virus Immune Globulin
Usage Information:
Rabies vaccine and HyperRAB S/D should be given to all persons suspected of exposure to rabies with one exception: persons who have been previously immunized with rabies vaccine and have a confirmed adequate rabies antibody titer should receive only vaccine. HyperRAB S/D should be administered as promptly as possible after exposure, but can be administered up to the eighth day after the first dose of vaccine is given.Recommendations for use of passive and active immunization after exposure to an animal suspected of having rabies have been detailed by the U.S. Public Health Service Advisory Committee on Immunization Practices (ACIP). [19]Every exposure to possible rabies infection must be individually evaluated. The following factors should be considered before specific antirabies treatment is initiated:
11-Digit NDC Billing Format:
13533061810
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1652827 - rabies immune globulin, human 150 UNT/ML in 2 ML Injection
  • RxCUI: 1652827 - 2 ML rabies immune globulin, human 150 UNT/ML Injection
  • RxCUI: 1652827 - rabies immune globulin, human 150 UNT/ML per 2 ML Injection
  • RxCUI: 1652830 - HyperRAB 150 UNT/ML in 2 ML Injection
  • RxCUI: 1652830 - 2 ML rabies immune globulin, human 150 UNT/ML Injection [HyperRAB]
  • Product Type:
    Plasma Derivative
    Labeler Name:
    Grifols Usa, Llc
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intramuscular - Administration within a muscle.
  • Sample Package:
    No
    FDA Application Number:
    BLA101144
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    08-14-1996
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    13533-618-021 VIAL, GLASS in 1 CARTON / 2 mL in 1 VIAL, GLASS (13533-618-20)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 13533-618-10?

    The NDC Packaged Code 13533-618-10 is assigned to a package of 1 vial in 1 carton / 10 ml in 1 vial (13533-618-11) of Hyperrab S/d, a plasma derivative labeled by Grifols Usa, Llc. The product's dosage form is injection and is administered via intramuscular form.

    Is NDC 13533-618 included in the NDC Directory?

    Yes, Hyperrab S/d with product code 13533-618 is active and included in the NDC Directory. The product was first marketed by Grifols Usa, Llc on August 14, 1996 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 NDC billing unit for package 13533-618-10?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 13533-618-10?

    The 11-digit format is 13533061810. 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
    5-3-213533-618-105-4-213533-0618-10