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  5. NDC Package Code: 71288-805-06 Isosulfan Blue

NDC Package 71288-805-06 Isosulfan Blue

Injection, Solution Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
71288-805-06
Package Description:
6 VIAL, SINGLE-DOSE in 1 CARTON / 5 mL in 1 VIAL, SINGLE-DOSE (71288-805-05)
Product Code:
71288-805
Proprietary Name:
Isosulfan Blue
Non-Proprietary Name:
Isosulfan Blue
Substance Name:
Isosulfan Blue
Usage Information:
Isosulfan blue 1% is contraindicated in those individuals with known hypersensitivity to triphenylmethane or related compounds.
11-Digit NDC Billing Format:
71288080506
Product Type:
Human Prescription Drug
Labeler Name:
Meitheal Pharmaceuticals Inc.
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):
  • ISOSULFAN BLUE 10 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    ANDA213130
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-03-2021
    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 71288-805-06?

    The NDC Packaged Code 71288-805-06 is assigned to a package of 6 vial, single-dose in 1 carton / 5 ml in 1 vial, single-dose (71288-805-05) of Isosulfan Blue, a human prescription drug labeled by Meitheal Pharmaceuticals Inc.. The product's dosage form is injection, solution and is administered via subcutaneous form.

    Is NDC 71288-805 included in the NDC Directory?

    Yes, Isosulfan Blue with product code 71288-805 is active and included in the NDC Directory. The product was first marketed by Meitheal Pharmaceuticals Inc. on November 03, 2021 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 71288-805-06?

    The 11-digit format is 71288080506. 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
    5-3-271288-805-065-4-271288-0805-06