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  5. NDC Package Code: 0008-1030-06 Rapamune

NDC Package 0008-1030-06 Rapamune

Sirolimus Solution Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    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:
0008-1030-06
Package Description:
1 CARTON in 1 KIT / 1 BOTTLE, GLASS in 1 CARTON (0008-1030-04) / 60 mL in 1 BOTTLE, GLASS
Product Code:
0008-1030
Proprietary Name:
Rapamune
Non-Proprietary Name:
Sirolimus
Substance Name:
Sirolimus
Usage Information:
Sirolimus is used with other medications to prevent rejection of a kidney transplant. This medication belongs to a class of drugs known as immunosuppressants. It works by weakening your body's defense system (immune system) to help your body accept the new organ as if it were your own. Sirolimus may also be used to treat a certain lung disease (lymphangioleiomyomatosis-LAM).
11-Digit NDC Billing Format:
00008103006
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 314230 - sirolimus 1 MG in 1 mL Oral Solution
  • RxCUI: 314230 - sirolimus 1 MG/ML Oral Solution
  • RxCUI: 314230 - sirolimus 1 MG per 1 ML Oral Solution
  • RxCUI: 349208 - sirolimus 1 MG Oral Tablet
  • RxCUI: 351901 - Rapamune 1 MG in 1 mL Oral Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.
    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):
  • SIROLIMUS 1 mg/mL
    • Pharmacologic Class(es):
  • Decreased Immunologic Activity - [PE] (Physiologic Effect)
  • Kinase Inhibitor - [EPC] (Established Pharmacologic Class)
  • Protein Kinase Inhibitors - [MoA] (Mechanism of Action)
  • mTOR Inhibitor Immunosuppressant - [EPC] (Established Pharmacologic Class)
  • mTOR Inhibitors - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    NDA021083
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    09-01-1999
    End Marketing Date:
    01-31-2025
    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.

    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 0008-1030-06 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    00008103006J7520Sirolimus, oral1 MG6016060

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0008-1030-06?

    The NDC Packaged Code 0008-1030-06 is assigned to a package of 1 carton in 1 kit / 1 bottle, glass in 1 carton (0008-1030-04) / 60 ml in 1 bottle, glass of Rapamune, a human prescription drug labeled by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.. The product's dosage form is solution and is administered via oral form.

    Is NDC 0008-1030 included in the NDC Directory?

    Yes, Rapamune with product code 0008-1030 is active and included in the NDC Directory. The product was first marketed by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc. on September 01, 1999.

    What is the NDC billing unit for package 0008-1030-06?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 0008-1030-06?

    The 11-digit format is 00008103006. 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
    4-4-20008-1030-065-4-200008-1030-06