NDC Package 0049-3920-83 Geodon

Ziprasidone Mesylate Injection, Powder, Lyophilized, For Solution Intramuscular - 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:
0049-3920-83
Package Description:
10 VIAL, SINGLE-DOSE in 1 CARTON / 1 mL in 1 VIAL, SINGLE-DOSE (0049-3920-20)
Product Code:
Proprietary Name:
Geodon
Non-Proprietary Name:
Ziprasidone Mesylate
Substance Name:
Ziprasidone Mesylate
Usage Information:
This medication is used to treat certain mental/mood disorders (schizophrenia, bipolar disorder). This medication can decrease hallucinations and help you to think more clearly and positively about yourself, feel less agitated, and take a more active part in everyday life. Ziprasidone belongs to a class of drugs called atypical antipsychotics. It works by helping to restore the balance of certain natural substances in the brain.
11-Digit NDC Billing Format:
00049392083
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 284548 - Geodon 40 MG Oral Capsule
  • RxCUI: 284548 - ziprasidone 40 MG Oral Capsule [Geodon]
  • RxCUI: 284548 - Geodon (as ziprasidone hydrochloride monohydrate) 40 MG Oral Capsule
  • RxCUI: 284549 - Geodon 60 MG Oral Capsule
  • RxCUI: 284549 - ziprasidone 60 MG Oral Capsule [Geodon]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Roerig
    Dosage Form:
    Injection, Powder, Lyophilized, For Solution - A dosage form intended for the solution prepared by lyophilization ("freeze drying"), a process which involves the removal of water from products in the frozen state at extremely low pressures; this is intended for subsequent addition of liquid to create a solution that conforms in all respects to the requirements for Injections.
    Administration Route(s):
  • Intramuscular - Administration within a muscle.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA020919
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    12-23-2003
    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.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 0049-3920-83 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    00049392083J3486Ziprasidone mesylate10 MG110220

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0049-3920-83?

    The NDC Packaged Code 0049-3920-83 is assigned to a package of 10 vial, single-dose in 1 carton / 1 ml in 1 vial, single-dose (0049-3920-20) of Geodon, a human prescription drug labeled by Roerig. The product's dosage form is injection, powder, lyophilized, for solution and is administered via intramuscular form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

    Is NDC 0049-3920 included in the NDC Directory?

    Yes, Geodon with product code 0049-3920 is active and included in the NDC Directory. The product was first marketed by Roerig on December 23, 2003 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 0049-3920-83?

    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 1.

    What is the 11-digit format for NDC 0049-3920-83?

    The 11-digit format is 00049392083. 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 4-4-2 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
    4-4-20049-3920-835-4-200049-3920-83