NDC Package 70748-173-26 Sevelamer Hydrochloride

Tablet 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:
70748-173-26
Package Description:
180 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Sevelamer Hydrochloride
Non-Proprietary Name:
Sevelamer Hydrochloride
Substance Name:
Sevelamer Hydrochloride
Usage Information:
Sevelamer hydrochloride tablets are indicated for the control of serum phosphorus in patients with chronic kidney disease (CKD) on dialysis. The safety and efficacy of sevelamer hydrochloride tablets in CKD patients who are not on dialysis have not been studied.
11-Digit NDC Billing Format:
70748017326
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
180 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 857216 - sevelamer HCl 400 MG Oral Tablet
  • RxCUI: 857216 - sevelamer hydrochloride 400 MG Oral Tablet
  • RxCUI: 857224 - sevelamer HCl 800 MG Oral Tablet
  • RxCUI: 857224 - sevelamer hydrochloride 800 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Lupin Pharmaceuticals, Inc.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA213145
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-25-2022
    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 70748-173-26?

    The NDC Packaged Code 70748-173-26 is assigned to a package of 180 tablet in 1 bottle of Sevelamer Hydrochloride, a human prescription drug labeled by Lupin Pharmaceuticals, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 70748-173 included in the NDC Directory?

    Yes, Sevelamer Hydrochloride with product code 70748-173 is active and included in the NDC Directory. The product was first marketed by Lupin Pharmaceuticals, Inc. on February 25, 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 70748-173-26?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 180.

    What is the 11-digit format for NDC 70748-173-26?

    The 11-digit format is 70748017326. 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
    5-3-270748-173-265-4-270748-0173-26