NDC Package 62135-968-41 Griseofulvin

Griseofulvin (microsize) Suspension Oral - 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:
62135-968-41
Package Description:
120 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Griseofulvin
Non-Proprietary Name:
Griseofulvin (microsize)
Substance Name:
Griseofulvin
Usage Information:
This medication is used to treat fungal infections of the skin, hair, and nails that do not respond to creams/lotions. Clearing such infections will get rid of symptoms such as itching, red/peeling/scaly skin, and discolored nails. This medication works by stopping the growth of fungi. It does not treat infections due to bacteria or yeast.
11-Digit NDC Billing Format:
62135096841
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
120 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 239238 - griseofulvin 125 MG in 5 mL Oral Suspension
  • RxCUI: 239238 - griseofulvin 25 MG/ML Oral Suspension
  • RxCUI: 239238 - griseofulvin 125 MG per 5 ML Oral Suspension
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Chartwell Rx, Llc.
    Dosage Form:
    Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA065200
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-02-2005
    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 62135-968-41?

    The NDC Packaged Code 62135-968-41 is assigned to a package of 120 ml in 1 bottle of Griseofulvin, a human prescription drug labeled by Chartwell Rx, Llc.. The product's dosage form is suspension and is administered via oral form.

    Is NDC 62135-968 included in the NDC Directory?

    Yes, Griseofulvin with product code 62135-968 is active and included in the NDC Directory. The product was first marketed by Chartwell Rx, Llc. on March 02, 2005 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 62135-968-41?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 120.

    What is the 11-digit format for NDC 62135-968-41?

    The 11-digit format is 62135096841. 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
    5-3-262135-968-415-4-262135-0968-41