NDC Package 55111-154-78 Ondansetron Hydrochloride

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:
55111-154-78
Package Description:
10 DOSE PACK in 1 BOX / 10 TABLET, FILM COATED in 1 DOSE PACK (55111-154-79)
Product Code:
Proprietary Name:
Ondansetron Hydrochloride
Non-Proprietary Name:
Ondansetron Hydrochloride
Substance Name:
Ondansetron Hydrochloride
Usage Information:
Prevention of nausea and vomiting associated with highly emetogenic cancer chemotherapy, including cisplatin ≥50 mg/m2.Prevention of nausea and vomiting associated with initial and repeat courses of moderately emetogenic cancer chemotherapy.Prevention of nausea and vomiting associated with radiotherapy in patients receiving either total body irradiation, single high-dose fraction to the abdomen, or daily fractions to the abdomen.Prevention of postoperative nausea and/or vomiting. As with other antiemetics, routine prophylaxis is not recommended for patients in whom there is little expectation that nausea and/or vomiting will occur postoperatively. In patients where nausea and/or vomiting must be avoided postoperatively, ondansetron tablets are recommended even where the incidence of postoperative nausea and/or vomiting is low.
11-Digit NDC Billing Format:
55111015478
NDC to RxNorm Crosswalk:
  • RxCUI: 198052 - ondansetron HCl 4 MG Oral Tablet
  • RxCUI: 198052 - ondansetron 4 MG Oral Tablet
  • RxCUI: 198052 - ondansetron 4 MG (as ondansetron HCl dihydrate 5 MG) Oral Tablet
  • RxCUI: 312084 - ondansetron 24 MG Oral Tablet
  • RxCUI: 312084 - ondansetron 24 MG (ondansetron hydrochloride dihydrate 30 MG) Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Dr. Reddy's Laboratories Limited
    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.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA076183
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-26-2006
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    55111-154-01100 TABLET, FILM COATED in 1 BOTTLE
    55111-154-05500 TABLET, FILM COATED in 1 BOTTLE
    55111-154-133 DOSE PACK in 1 BOX / 1 TABLET, FILM COATED in 1 DOSE PACK
    55111-154-3030 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 55111-154-78?

    The NDC Packaged Code 55111-154-78 is assigned to a package of 10 dose pack in 1 box / 10 tablet, film coated in 1 dose pack (55111-154-79) of Ondansetron Hydrochloride, a human prescription drug labeled by Dr. Reddy's Laboratories Limited. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 55111-154 included in the NDC Directory?

    Yes, Ondansetron Hydrochloride with product code 55111-154 is active and included in the NDC Directory. The product was first marketed by Dr. Reddy's Laboratories Limited on December 26, 2006 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 55111-154-78?

    The 11-digit format is 55111015478. 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
    5-3-255111-154-785-4-255111-0154-78