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  5. NDC Package Code: 37945-908-12 Fungistat Max

NDC Package 37945-908-12 Fungistat Max

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
37945-908-12
Package Description:
1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE (37945-908-13)
Product Code:
37945-908
Proprietary Name:
Fungistat Max
Usage Information:
Cures most tinea pedis (athlete's foot), tinea cruris (jock itch), and tinea corporis (ringworm).Relieves itching, burning feet and itching, scaling, cracking, burning, redness, soreness, irritation, discomfort, and chafing associated with jock itch.Clears up most athlete’s foot infection and with daily use helps keep it from coming back.
11-Digit NDC Billing Format:
37945090812
NDC to RxNorm Crosswalk:
  • RxCUI: 1747489 - FUNGISTAT MAX 1 % Topical Solution
  • RxCUI: 1747489 - clotrimazole 10 MG/ML Topical Solution [Fungistat]
  • RxCUI: 1747489 - Fungistat 10 MG/ML Topical Solution
  • RxCUI: 1747489 - Fungistat Max 1 % Topical Solution
  • RxCUI: 309370 - clotrimazole 1 % Topical Solution
    • Labeler Name:
    Bio-medical & Pharmaceutical Manufacturing Corporation
    Sample Package:
    No
    Start Marketing Date:
    04-12-2016
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    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 37945-908-12?

    The NDC Packaged Code 37945-908-12 is assigned to a package of 1 bottle in 1 box / 30 ml in 1 bottle (37945-908-13) of Fungistat Max, labeled by Bio-medical & Pharmaceutical Manufacturing Corporation. The product's dosage form is and is administered via form.

    Is NDC 37945-908 included in the NDC Directory?

    No, Fungistat Max with product code 37945-908 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Bio-medical & Pharmaceutical Manufacturing Corporation on April 12, 2016 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 37945-908-12?

    The 11-digit format is 37945090812. 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
    5-3-237945-908-125-4-237945-0908-12