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  5. NDC Package Code: 51991-735-20 Granisetron Hydrochloride

NDC Package 51991-735-20 Granisetron Hydrochloride

Tablet 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:
51991-735-20
Package Description:
2 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
Product Code:
51991-735
Proprietary Name:
Granisetron Hydrochloride
Non-Proprietary Name:
Granisetron Hydrochloride
Substance Name:
Granisetron Hydrochloride
Usage Information:
Granisetron hydrochloride tablets USP are indicated for the prevention of:Nausea and vomiting associated with initial and repeat courses of emetogenic cancer therapy, including high-dose cisplatin.Nausea and vomiting associated with radiation, including total body irradiation and fractionated abdominal radiation.
11-Digit NDC Billing Format:
51991073520
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
2 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 310599 - granisetron HCl 1 MG Oral Tablet
  • RxCUI: 310599 - granisetron 1 MG Oral Tablet
  • RxCUI: 310599 - granisetron 1 MG (granisetron hydrochloride 1.12 MG) Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Breckenridge Pharmaceutical, 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):
  • GRANISETRON HYDROCHLORIDE 1 mg/1
    • Pharmacologic Class(es):
  • Serotonin 3 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Serotonin-3 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA078969
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-22-2009
    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
    51991-735-321 BLISTER PACK in 1 CARTON / 2 TABLET in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51991-735-20?

    The NDC Packaged Code 51991-735-20 is assigned to a package of 2 blister pack in 1 carton / 10 tablet in 1 blister pack of Granisetron Hydrochloride, a human prescription drug labeled by Breckenridge Pharmaceutical, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 51991-735 included in the NDC Directory?

    Yes, Granisetron Hydrochloride with product code 51991-735 is active and included in the NDC Directory. The product was first marketed by Breckenridge Pharmaceutical, Inc. on June 22, 2009 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 NDC billing unit for package 51991-735-20?

    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 2.

    What is the 11-digit format for NDC 51991-735-20?

    The 11-digit format is 51991073520. 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
    5-3-251991-735-205-4-251991-0735-20