NDC Package 0004-0800-07 Tamiflu

Oseltamivir Phosphate Capsule 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:
0004-0800-07
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 10 CAPSULE in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Tamiflu
Non-Proprietary Name:
Oseltamivir Phosphate
Substance Name:
Oseltamivir Phosphate
Usage Information:
Oseltamivir is used to treat symptoms caused by the flu virus (influenza). It helps make the symptoms (such as stuffy nose, cough, sore throat, fever/chills, aches, tiredness) less severe and shortens the recovery time by 1-2 days. This medication may also be used to prevent the flu if you have been exposed to someone who already has the flu (such as a sick household member) or if there is a flu outbreak in the community. Talk to your doctor for more details. This medication works by stopping the flu virus from growing. It is not a substitute for the flu vaccine. (See also Notes section.)
11-Digit NDC Billing Format:
00004080007
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: 1115698 - oseltamivir phosphate 6 MG in 1 mL Oral Suspension
  • RxCUI: 1115698 - oseltamivir 6 MG/ML Oral Suspension
  • RxCUI: 1115698 - oseltamivir (as oseltamivir phosphate) 6 MG/ML Oral Suspension
  • RxCUI: 1115698 - oseltamivir phosphate 6 MG per 1 ML Oral Suspension
  • RxCUI: 1115700 - Tamiflu 6 MG in 1 mL Oral Suspension
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Genentech, Inc.
    Dosage Form:
    Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA021087
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    10-27-1999
    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
    0004-0800-081 BOTTLE, PLASTIC in 1 CARTON / 10 CAPSULE in 1 BOTTLE, PLASTIC
    0004-0800-851 BLISTER PACK in 1 CARTON / 10 CAPSULE in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0004-0800-07?

    The NDC Packaged Code 0004-0800-07 is assigned to a package of 1 bottle, plastic in 1 carton / 10 capsule in 1 bottle, plastic of Tamiflu, a human prescription drug labeled by Genentech, Inc.. The product's dosage form is capsule and is administered via oral form.

    Is NDC 0004-0800 included in the NDC Directory?

    Yes, Tamiflu with product code 0004-0800 is active and included in the NDC Directory. The product was first marketed by Genentech, Inc. on October 27, 1999 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 0004-0800-07?

    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 0004-0800-07?

    The 11-digit format is 00004080007. 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
    4-4-20004-0800-075-4-200004-0800-07