NDC Package 31722-837-10 Valganciclovir

Valganciclovir Hydrochloride Powder, For Solution 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:
31722-837-10
Package Description:
1 BOTTLE, GLASS in 1 CARTON / 100 mL in 1 BOTTLE, GLASS
Product Code:
Proprietary Name:
Valganciclovir
Non-Proprietary Name:
Valganciclovir Hydrochloride
Substance Name:
Valganciclovir Hydrochloride
Usage Information:
Valganciclovir for oral solution is contraindicated in patients who have had a demonstrated clinically significant hypersensitivity reaction (e.g., anaphylaxis) to valganciclovir, ganciclovir, or any component of the formulation [see Adverse Reactions ( 6.1)].
11-Digit NDC Billing Format:
31722083710
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 863559 - valGANciclovir 50 MG in 1 mL Oral Solution
  • RxCUI: 863559 - valganciclovir 50 MG/ML Oral Solution
  • RxCUI: 863559 - valganciclovir (as valganciclovir hydrochloride) 50 MG/ML Oral Solution
  • RxCUI: 863559 - valganciclovir 50 MG per 1 ML Oral Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Camber Pharmaceuticals, Inc.
    Dosage Form:
    Powder, For Solution - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a solution.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA211475
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-04-2022
    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 31722-837-10?

    The NDC Packaged Code 31722-837-10 is assigned to a package of 1 bottle, glass in 1 carton / 100 ml in 1 bottle, glass of Valganciclovir, a human prescription drug labeled by Camber Pharmaceuticals, Inc.. The product's dosage form is powder, for solution and is administered via oral form.

    Is NDC 31722-837 included in the NDC Directory?

    Yes, Valganciclovir with product code 31722-837 is active and included in the NDC Directory. The product was first marketed by Camber Pharmaceuticals, Inc. on October 04, 2022 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 31722-837-10?

    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 31722-837-10?

    The 11-digit format is 31722083710. 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
    5-3-231722-837-105-4-231722-0837-10