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  5. NDC Package Code: 60492-0075-2 Bat

NDC Package 60492-0075-2 Bat

Botulism Antitoxin Heptavalent Liquid Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
60492-0075-2
Package Description:
50 mL in 1 VIAL, GLASS
Product Code:
60492-0075
Proprietary Name:
Bat
Non-Proprietary Name:
Botulism Antitoxin Heptavalent
Substance Name:
Equine Botulinum Neurotoxin A Immune Fab2; Equine Botulinum Neurotoxin B Immune Fab2; Equine Botulinum Neurotoxin C Immune Fab2; Equine Botulinum Neurotoxin D Immune Fab2; Equine Botulinum Neurotoxin E Immune Fab2; Equine Botulinum Neurotoxin F Immune Fab2; Equine Botulinum Neurotoxin G Immune Fab2
Usage Information:
BAT [Botulism Antitoxin Heptavalent (A, B, C, D, E, F, G) – (Equine)] is a mixture of immune globulin fragments indicated for the treatment of symptomatic botulism following documented or suspected exposure to botulinum neurotoxin serotypes A, B, C, D, E, F, or G in adults and pediatric patients.The effectiveness of BAT is based on efficacy studies conducted in animal models of botulism.
11-Digit NDC Billing Format:
60492007502
NDC to RxNorm Crosswalk:
  • RxCUI: 1722719 - botulism antitoxin heptavalent (A, B, C, D, E, F, G), Equine Injection
  • RxCUI: 1722719 - botulinum neurotoxin A immune FAB2, equine 4500 UNT / botulinum neurotoxin B immune FAB2, equine 3300 UNT / botulinum neurotoxin C immune FAB2, equine 3000 UNT / botulinum neurotoxin D immune FAB2, equine 600 UNT / botulinum neurotoxin E immune FAB2, equine 5100 UNT / botulinum neurotoxin F immune FAB2, equine 3000 UNT / botulinum neurotoxin G immune FAB2, equine 600 UNT Injection
    • Product Type:
    Plasma Derivative
    Labeler Name:
    Emergent Biosolutions Canada Inc.
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • EQUINE BOTULINUM NEUROTOXIN A IMMUNE FAB2 4500 [iU]/10mL
  • EQUINE BOTULINUM NEUROTOXIN B IMMUNE FAB2 3300 [iU]/10mL
  • EQUINE BOTULINUM NEUROTOXIN C IMMUNE FAB2 3000 [iU]/10mL
  • EQUINE BOTULINUM NEUROTOXIN D IMMUNE FAB2 600 [iU]/10mL
  • EQUINE BOTULINUM NEUROTOXIN E IMMUNE FAB2 5100 [iU]/10mL
  • EQUINE BOTULINUM NEUROTOXIN F IMMUNE FAB2 3000 [iU]/10mL
  • EQUINE BOTULINUM NEUROTOXIN G IMMUNE FAB2 600 [iU]/10mL
    • Sample Package:
    No
    FDA Application Number:
    BLA125462
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    03-01-2013
    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
    60492-0075-320 mL in 1 VIAL, GLASS
    60492-0075-450 mL in 1 VIAL, GLASS

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 60492-0075-2?

    The NDC Packaged Code 60492-0075-2 is assigned to a package of 50 ml in 1 vial, glass of Bat, a plasma derivative labeled by Emergent Biosolutions Canada Inc.. The product's dosage form is liquid and is administered via intravenous form.

    Is NDC 60492-0075 included in the NDC Directory?

    Yes, Bat with product code 60492-0075 is active and included in the NDC Directory. The product was first marketed by Emergent Biosolutions Canada Inc. on March 01, 2013 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 60492-0075-2?

    The 11-digit format is 60492007502. 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 5-4-1 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
    5-4-160492-0075-25-4-260492-0075-02