NDC Package 68999-417-46 Doxycycline

Powder, For Suspension 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:
68999-417-46
Package Description:
60 mL in 1 BOTTLE, GLASS
Product Code:
Proprietary Name:
Doxycycline
Non-Proprietary Name:
Doxycycline
Substance Name:
Doxycycline
Usage Information:
To reduce the development of drug-resistant bacteria and maintain effectiveness of Doxycycline Hyclate Capsules and other antibacterial drugs, Doxycycline Hyclate Capsules should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.
11-Digit NDC Billing Format:
68999041746
NDC to RxNorm Crosswalk:
  • RxCUI: 1649405 - doxycycline hyclate 50 MG Oral Capsule
  • RxCUI: 1649988 - doxycycline hyclate 100 MG Oral Capsule
  • RxCUI: 1649988 - doxycycline (as doxycycline hyclate) 100 MG Oral Capsule
  • RxCUI: 1650030 - doxycycline monohydrate 25 MG in 5 mL Oral Suspension
  • RxCUI: 1650030 - doxycycline monohydrate 5 MG/ML Oral Suspension
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Chartwell Governmental & Specialty Rx, Llc
    Dosage Form:
    Powder, For Suspension - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a suspension (a liquid preparation containing the solid particles dispersed in the liquid vehicle).
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA065454
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-16-2008
    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.

    Frequently Asked Questions

    What is NDC 68999-417-46?

    The NDC Packaged Code 68999-417-46 is assigned to a package of 60 ml in 1 bottle, glass of Doxycycline, a human prescription drug labeled by Chartwell Governmental & Specialty Rx, Llc. The product's dosage form is powder, for suspension and is administered via oral form.

    Is NDC 68999-417 included in the NDC Directory?

    Yes, Doxycycline with product code 68999-417 is active and included in the NDC Directory. The product was first marketed by Chartwell Governmental & Specialty Rx, Llc on July 16, 2008 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 11-digit format for NDC 68999-417-46?

    The 11-digit format is 68999041746. 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
    5-3-268999-417-465-4-268999-0417-46