NDC Package 0135-7021-02 Panadol PM

Acetaminophen And Diphenhydramine Hcl 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:
0135-7021-02
Package Description:
1 BOTTLE in 1 CARTON / 24 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Panadol PM
Non-Proprietary Name:
Acetaminophen And Diphenhydramine Hcl
Substance Name:
Acetaminophen; Diphenhydramine Hydrochloride
Usage Information:
•do not take more than directed (see overdose warning)•adults and children 12 years of age and over: take 2 caplets at bedtime, if needed, or as directed by a doctor•do not give to children under 12 years of age
11-Digit NDC Billing Format:
00135702102
NDC to RxNorm Crosswalk:
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG Oral Tablet
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet
  • RxCUI: 1092189 - APAP 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet
  • RxCUI: 1094718 - Panadol PM EXTRA STRENGTH 500 MG / 25 MG Oral Tablet
  • RxCUI: 1094718 - acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet [Panadol PM]
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Haleon Us Holdings Llc
    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:
    M013
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-25-2021
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0135-7021-0150 PACKET in 1 CARTON / 2 TABLET, FILM COATED in 1 PACKET
    0135-7021-031 BOTTLE in 1 CARTON / 50 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0135-7021-02?

    The NDC Packaged Code 0135-7021-02 is assigned to a package of 1 bottle in 1 carton / 24 tablet, film coated in 1 bottle of Panadol PM, a human over the counter drug labeled by Haleon Us Holdings Llc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 0135-7021 included in the NDC Directory?

    Yes, Panadol PM with product code 0135-7021 is active and included in the NDC Directory. The product was first marketed by Haleon Us Holdings Llc on June 25, 2021 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 0135-7021-02?

    The 11-digit format is 00135702102. 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
    4-4-20135-7021-025-4-200135-7021-02