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  5. NDC Package Code: 50436-3250-3 Valacyclovir Hydrochloride

NDC Package 50436-3250-3 Valacyclovir Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
50436-3250-3
Package Description:
90 TABLET, FILM COATED in 1 BOTTLE
Product Code:
50436-3250
Proprietary Name:
Valacyclovir Hydrochloride
Usage Information:
Valacyclovir hydrochloride is contraindicated in patients who have had a demonstrated clinically significant hypersensitivity reaction (e.g., anaphylaxis) to valacyclovir, acyclovir, or any component of the formulation [see Adverse Reactions (6.3)].
11-Digit NDC Billing Format:
50436325003
NDC to RxNorm Crosswalk:
  • RxCUI: 313564 - valACYclovir 1 GM Oral Tablet
  • RxCUI: 313564 - valacyclovir 1000 MG Oral Tablet
  • RxCUI: 313564 - valacyclovir (as valacyclovir HCl) 1 GM Oral Tablet
  • RxCUI: 313564 - valacyclovir 1 GM Oral Tablet
  • RxCUI: 313565 - valACYclovir 500 MG Oral Tablet
    • Labeler Name:
    Unit Dose Services
    Sample Package:
    No
    Start Marketing Date:
    04-05-2012
    Listing Expiration Date:
    12-31-2020
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    50436-3250-130 TABLET, FILM COATED in 1 BOTTLE
    50436-3250-412 TABLET, FILM COATED in 1 BOTTLE
    50436-3250-515 TABLET, FILM COATED in 1 BOTTLE
    50436-3250-624 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50436-3250-3?

    The NDC Packaged Code 50436-3250-3 is assigned to a package of 90 tablet, film coated in 1 bottle of Valacyclovir Hydrochloride, labeled by Unit Dose Services. The product's dosage form is and is administered via form.

    Is NDC 50436-3250 included in the NDC Directory?

    No, Valacyclovir Hydrochloride with product code 50436-3250 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Unit Dose Services on April 05, 2012 and its listing in the NDC Directory is set to expire on December 31, 2020 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50436-3250-3?

    The 11-digit format is 50436325003. 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 5-4-1 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
    5-4-150436-3250-35-4-250436-3250-03