NDC Package 68094-043-62 Sucralfate

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:
68094-043-62
Package Description:
3 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (68094-043-59)
Product Code:
Proprietary Name:
Sucralfate
Non-Proprietary Name:
Sucralfate
Substance Name:
Sucralfate
Usage Information:
This medication is used to treat and prevent ulcers in the intestines. Sucralfate forms a coating over ulcers, protecting the area from further injury. This helps ulcers heal more quickly.
11-Digit NDC Billing Format:
68094004362
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 313123 - sucralfate 1 GM in 10 mL Oral Suspension
  • RxCUI: 313123 - sucralfate 100 MG/ML Oral Suspension
  • RxCUI: 313123 - sucralfate 1 GM per 10 ML Oral Suspension
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Precision Dose, Inc.
    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:
    NDA019183
    Marketing Category:
    NDA AUTHORIZED GENERIC - A product marketed as a "generic" drug under an approved New Drug Application (NDA), rather than an Abbreviated New Drug Application (ANDA),.
    Start Marketing Date:
    03-19-2020
    End Marketing Date:
    02-28-2025
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    68094-043-6110 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (68094-043-59)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68094-043-62?

    The NDC Packaged Code 68094-043-62 is assigned to a package of 3 tray in 1 case / 10 cup, unit-dose in 1 tray / 10 ml in 1 cup, unit-dose (68094-043-59) of Sucralfate, a human prescription drug labeled by Precision Dose, Inc.. The product's dosage form is suspension and is administered via oral form.

    Is NDC 68094-043 included in the NDC Directory?

    Yes, Sucralfate with product code 68094-043 is active and included in the NDC Directory. The product was first marketed by Precision Dose, Inc. on March 19, 2020.

    What is the NDC billing unit for package 68094-043-62?

    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 68094-043-62?

    The 11-digit format is 68094004362. 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
    5-3-268094-043-625-4-268094-0043-62