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  5. NDC Package Code: 0002-6145-27 Baqsimi

NDC Package 0002-6145-27 Baqsimi

Glucagon Powder Nasal - 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:
0002-6145-27
Package Description:
2 TUBE in 1 CARTON / 1 BOTTLE, UNIT-DOSE in 1 TUBE (0002-6145-02) / 1 POWDER in 1 BOTTLE, UNIT-DOSE (0002-6145-01)
Product Code:
0002-6145
Proprietary Name:
Baqsimi
Non-Proprietary Name:
Glucagon
Substance Name:
Glucagon
Usage Information:
This medication is the same as your body's own glucagon, a natural substance that raises blood sugar by causing the body to release sugar stored in the liver. It is used to treat very low blood sugar (hypoglycemia) that may cause you to need help from others. Make sure a family member or caregiver knows where you keep this medication and how to use it before you need their help.
11-Digit NDC Billing Format:
00002614527
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
2 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 2180666 - glucagon 3 MG Nasal Powder
  • RxCUI: 2180671 - baqsimi 3 MG Nasal Powder
  • RxCUI: 2180671 - glucagon 3 MG Nasal Powder [Baqsimi]
  • RxCUI: 2180671 - Baqsimi 3 MG Nasal Powder
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Eli Lilly And Company
    Dosage Form:
    Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
    Administration Route(s):
  • Nasal - Administration to the nose; administered by way of the nose.
    • Active Ingredient(s):
  • GLUCAGON 3 mg/1
    • Pharmacologic Class(es):
  • Antihypoglycemic Agent - [EPC] (Established Pharmacologic Class)
  • Decreased GI Motility - [PE] (Physiologic Effect)
  • Decreased GI Smooth Muscle Tone - [PE] (Physiologic Effect)
  • Decreased Glycolysis - [PE] (Physiologic Effect)
  • Gastrointestinal Motility Inhibitor - [EPC] (Established Pharmacologic Class)
  • Increased Gluconeogenesis - [PE] (Physiologic Effect)
  • Increased Glycogenolysis - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    NDA210134
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    07-24-2019
    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
    0002-6145-111 TUBE in 1 CARTON / 1 BOTTLE, UNIT-DOSE in 1 TUBE (0002-6145-02) / 1 POWDER in 1 BOTTLE, UNIT-DOSE (0002-6145-01)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0002-6145-27?

    The NDC Packaged Code 0002-6145-27 is assigned to a package of 2 tube in 1 carton / 1 bottle, unit-dose in 1 tube (0002-6145-02) / 1 powder in 1 bottle, unit-dose (0002-6145-01) of Baqsimi, a human prescription drug labeled by Eli Lilly And Company. The product's dosage form is powder and is administered via nasal form.

    Is NDC 0002-6145 included in the NDC Directory?

    Yes, Baqsimi with product code 0002-6145 is active and included in the NDC Directory. The product was first marketed by Eli Lilly And Company on July 24, 2019 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 0002-6145-27?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 2.

    What is the 11-digit format for NDC 0002-6145-27?

    The 11-digit format is 00002614527. 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
    4-4-20002-6145-275-4-200002-6145-27