NDC Package 42708-036-30 Losartan Potassium And Hydrochlorothiazide

Tablet, Film Coated 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:
42708-036-30
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Losartan Potassium And Hydrochlorothiazide
Non-Proprietary Name:
Losartan Potassium And Hydrochlorothiazide
Substance Name:
Hydrochlorothiazide; Losartan Potassium
Usage Information:
Losartan potassium and hydrochlorothiazide tablets are contraindicated:•In patients who are hypersensitive to any component of this product.•In patients with anuria•For coadministration with aliskiren in patients with diabetes
11-Digit NDC Billing Format:
42708003630
NDC to RxNorm Crosswalk:
  • RxCUI: 979468 - losartan potassium 50 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
  • RxCUI: 979468 - hydrochlorothiazide 12.5 MG / losartan potassium 50 MG Oral Tablet
  • RxCUI: 979468 - HCTZ 12.5 MG / Losartan K+ 50 MG Oral Tablet
  • RxCUI: 979468 - HCTZ 12.5 MG / Losartan Pot 50 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Qpharma Inc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    Yes
    FDA Application Number:
    ANDA077157
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-06-2010
    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 42708-036-30?

    The NDC Packaged Code 42708-036-30 is assigned to a package of 30 tablet, film coated in 1 bottle of Losartan Potassium And Hydrochlorothiazide, a human prescription drug labeled by Qpharma Inc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 42708-036 included in the NDC Directory?

    Yes, Losartan Potassium And Hydrochlorothiazide with product code 42708-036 is active and included in the NDC Directory. The product was first marketed by Qpharma Inc on April 06, 2010 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 11-digit format for NDC 42708-036-30?

    The 11-digit format is 42708003630. 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
    5-3-242708-036-305-4-242708-0036-30