NDC Package 69539-006-31 Moxifloxacin Hydrochloride Tablets, 400 Mg

Tablet, Film Coated 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:
69539-006-31
Package Description:
50 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK (69539-006-11)
Product Code:
Proprietary Name:
Moxifloxacin Hydrochloride Tablets, 400 Mg
Non-Proprietary Name:
Moxifloxacin Hydrochloride Tablets, 400 Mg
Substance Name:
Moxifloxacin Hydrochloride Monohydrate
Usage Information:
Moxifloxacin hydrochloride is contraindicated in persons with a history of hypersensitivity to moxifloxacin or any member of the quinolone class of antibacterials [see Warnings and Precautions (5.8)].
11-Digit NDC Billing Format:
69539000631
NDC to RxNorm Crosswalk:
  • RxCUI: 311787 - moxifloxacin HCl 400 MG Oral Tablet
  • RxCUI: 311787 - moxifloxacin 400 MG Oral Tablet
  • RxCUI: 311787 - moxifloxacin (as moxifloxacin HCl) 400 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Msn Laboratories Private Limited
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA208682
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-22-2017
    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
    69539-006-05500 TABLET, FILM COATED in 1 BOTTLE
    69539-006-3030 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69539-006-31?

    The NDC Packaged Code 69539-006-31 is assigned to a package of 50 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack (69539-006-11) of Moxifloxacin Hydrochloride Tablets, 400 Mg, a human prescription drug labeled by Msn Laboratories Private Limited. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 69539-006 included in the NDC Directory?

    Yes, Moxifloxacin Hydrochloride Tablets, 400 Mg with product code 69539-006 is active and included in the NDC Directory. The product was first marketed by Msn Laboratories Private Limited on September 22, 2017 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 69539-006-31?

    The 11-digit format is 69539000631. 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
    5-3-269539-006-315-4-269539-0006-31