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  5. NDC Package Code: 0088-2502-05 Apidra Solostar

NDC Package 0088-2502-05 Apidra Solostar

Insulin Glulisine Injection, Solution Subcutaneous - 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:
0088-2502-05
Package Description:
5 SYRINGE, PLASTIC in 1 CARTON / 3 mL in 1 SYRINGE, PLASTIC (0088-2502-00)
Product Code:
0088-2502
Proprietary Name:
Apidra Solostar
Non-Proprietary Name:
Insulin Glulisine
Substance Name:
Insulin Glulisine
Usage Information:
Insulin glulisine is used with a proper diet and exercise program to control high blood sugar in people with diabetes. Controlling high blood sugar helps prevent kidney damage, blindness, nerve problems, loss of limbs, and sexual function problems. Proper control of diabetes may also lessen your risk of a heart attack or stroke. Insulin glulisine is a man-made product that is similar to human insulin. It replaces the insulin that your body would normally make. Insulin glulisine starts working faster and lasts for a shorter time than regular insulin. It works by helping blood sugar (glucose) get into cells so your body can use it for energy. This medication is usually used with a medium- or long-acting insulin product.
11-Digit NDC Billing Format:
00088250205
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 485210 - insulin glulisine 100 UNT/ML Injectable Solution
  • RxCUI: 485210 - insulin glulisine, human 100 UNT/ML Injectable Solution
  • RxCUI: 485210 - insulin analog, glulisine 100 UNT/ML Injectable Solution
  • RxCUI: 803194 - Apidra 100 UNT/ML Injectable Solution
  • RxCUI: 803194 - insulin glulisine, human 100 UNT/ML Injectable Solution [Apidra]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sanofi-aventis U.s. Llc
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
    • Active Ingredient(s):
  • INSULIN GLULISINE 100 [iU]/mL
    • Pharmacologic Class(es):
  • Insulin Analog - [EPC] (Established Pharmacologic Class)
  • Insulin - [Chemical/Ingredient]
    • Sample Package:
    No
    FDA Application Number:
    BLA021629
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    02-24-2009
    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
    0088-2502-011 SYRINGE, PLASTIC in 1 CARTON / 3 mL in 1 SYRINGE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0088-2502-05?

    The NDC Packaged Code 0088-2502-05 is assigned to a package of 5 syringe, plastic in 1 carton / 3 ml in 1 syringe, plastic (0088-2502-00) of Apidra Solostar, a human prescription drug labeled by Sanofi-aventis U.s. Llc. The product's dosage form is injection, solution and is administered via subcutaneous form.

    Is NDC 0088-2502 included in the NDC Directory?

    Yes, Apidra Solostar with product code 0088-2502 is active and included in the NDC Directory. The product was first marketed by Sanofi-aventis U.s. Llc on February 24, 2009 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 0088-2502-05?

    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 0088-2502-05?

    The 11-digit format is 00088250205. 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
    4-4-20088-2502-055-4-200088-2502-05