NDC Package 75907-023-48 Clonidine

Patch, Extended Release Transdermal - 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:
75907-023-48
Package Description:
4 POUCH in 1 CARTON / 1 PATCH in 1 POUCH (75907-023-11) / 24 h in 1 PATCH
Product Code:
Proprietary Name:
Clonidine
Non-Proprietary Name:
Clonidine
Substance Name:
Clonidine
Usage Information:
This medication is used alone or with other medications to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. Clonidine belongs to a class of drugs (central alpha agonists) that act in the brain to lower blood pressure. It works by relaxing blood vessels so blood can flow more easily.
11-Digit NDC Billing Format:
75907002348
NDC to RxNorm Crosswalk:
  • RxCUI: 998671 - cloNIDine HCl 0.1 MG/Day Weekly Transdermal System
  • RxCUI: 998671 - 168 HR clonidine 0.00417 MG/HR Transdermal System
  • RxCUI: 998671 - clonidine HCl 0.1 MG/Day Weekly Transdermal System
  • RxCUI: 998671 - clonidine hydrochloride 0.1 MG/Day Weekly Transdermal Patch
  • RxCUI: 998675 - cloNIDine HCl 0.2 MG/Day Weekly Transdermal System
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Dr. Reddy's Labratories Inc.
    Dosage Form:
    Patch, Extended Release - A drug delivery system in the form of a patch that releases the drug in such a manner that a reduction in dosing frequency compared to that drug presented as a conventional dosage form (e.g., a solution or a prompt drug-releasing, conventional solid dosage form).
    Administration Route(s):
  • Transdermal - Administration through the dermal layer of the skin to the systemic circulation by diffusion.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA079090
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-10-2024
    Listing Expiration Date:
    12-31-2025
    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.

    Frequently Asked Questions

    What is NDC 75907-023-48?

    The NDC Packaged Code 75907-023-48 is assigned to a package of 4 pouch in 1 carton / 1 patch in 1 pouch (75907-023-11) / 24 h in 1 patch of Clonidine, a human prescription drug labeled by Dr. Reddy's Labratories Inc.. The product's dosage form is patch, extended release and is administered via transdermal form.

    Is NDC 75907-023 included in the NDC Directory?

    Yes, Clonidine with product code 75907-023 is active and included in the NDC Directory. The product was first marketed by Dr. Reddy's Labratories Inc. on February 10, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 75907-023-48?

    The 11-digit format is 75907002348. 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
    5-3-275907-023-485-4-275907-0023-48