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  5. NDC Package Code: 80056-801-30 Granisol

NDC Package 80056-801-30 Granisol

Granisetron Hydrochloride Solution Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
80056-801-30
Package Description:
30 mL in 1 BOTTLE, GLASS
Product Code:
80056-801
Proprietary Name:
Granisol
Non-Proprietary Name:
Granisetron Hydrochloride
Substance Name:
Granisetron Hydrochloride
Usage Information:
Granisetron is 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:
80056080130
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Intra-sana Laboratories
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
GRANISETRON HYDROCHLORIDE 2 mg/10mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA219282
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
07-04-2025
Listing Expiration Date:
12-31-2026
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 80056-801-30?

The NDC Packaged Code 80056-801-30 is assigned to a package of 30 ml in 1 bottle, glass of Granisol, a human prescription drug labeled by Intra-sana Laboratories. The product's dosage form is solution and is administered via oral form.

Is NDC 80056-801 included in the NDC Directory?

Yes, Granisol with product code 80056-801 is active and included in the NDC Directory. The product was first marketed by Intra-sana Laboratories on July 04, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 80056-801-30?

The 11-digit format is 80056080130. 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
5-3-280056-801-305-4-280056-0801-30