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  5. NDC Package Code: 58914-170-60 Carafate

NDC Package 58914-170-60 Carafate

Sucralfate Suspension Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
58914-170-60
Package Description:
6 CUP, UNIT-DOSE in 1 BOX / 10 mL in 1 CUP, UNIT-DOSE
Product Code:
58914-170
Proprietary Name:
Carafate
Non-Proprietary Name:
Sucralfate
Substance Name:
Sucralfate
Usage Information:
This medication is used to treat 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:
58914017060
NDC to RxNorm Crosswalk:
  • RxCUI: 208094 - Carafate 1 GM in 10 mL Oral Suspension
  • RxCUI: 208094 - sucralfate 100 MG/ML Oral Suspension [Carafate]
  • RxCUI: 208094 - Carafate 1 GM per 10 ML Oral Suspension
  • RxCUI: 208094 - Carafate 100 MG/ML Oral Suspension
  • RxCUI: 313123 - sucralfate 1 GM in 10 mL Oral Suspension
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Allergan, 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):
  • SUCRALFATE 1 g/10mL
    • Pharmacologic Class(es):
  • Aluminum Complex - [EPC] (Established Pharmacologic Class)
  • Organometallic Compounds - [CS]
    • Sample Package:
    Yes
    FDA Application Number:
    NDA019183
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    12-16-1993
    Listing Expiration Date:
    12-31-2025
    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
    58914-170-14420 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 58914-170-60?

    The NDC Packaged Code 58914-170-60 is assigned to a package of 6 cup, unit-dose in 1 box / 10 ml in 1 cup, unit-dose of Carafate, a human prescription drug labeled by Allergan, Inc.. The product's dosage form is suspension and is administered via oral form.

    Is NDC 58914-170 included in the NDC Directory?

    Yes, Carafate with product code 58914-170 is active and included in the NDC Directory. The product was first marketed by Allergan, Inc. on December 16, 1993 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 58914-170-60?

    The 11-digit format is 58914017060. 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
    5-3-258914-170-605-4-258914-0170-60