NDC Package 29485-7963-2 Benadryl

Diphenhydramine Hydrochloride 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:
29485-7963-2
Package Description:
25 POUCH in 1 BOX / 2 TABLET, FILM COATED in 1 POUCH
Product Code:
Proprietary Name:
Benadryl
Non-Proprietary Name:
Diphenhydramine Hydrochloride
Substance Name:
Diphenhydramine Hydrochloride
Usage Information:
Take every 4 to 6 hours, or as directed by a doctordo not take more than 6 times in 24 hoursadults and children 12 years and over1 to 2 tabletschildren 6 to under 12 years1 tabletchildren under 6 yearsdo not use
11-Digit NDC Billing Format:
29485796302
NDC to RxNorm Crosswalk:
  • RxCUI: 1049630 - diphenhydrAMINE HCl 25 MG Oral Tablet
  • RxCUI: 1049630 - diphenhydramine hydrochloride 25 MG Oral Tablet
  • RxCUI: 1049632 - Benadryl 25 MG Oral Tablet
  • RxCUI: 1049632 - diphenhydramine hydrochloride 25 MG Oral Tablet [Benadryl]
  • RxCUI: 1049632 - Benadryl Allergy Ultratab 25 MG Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Lil' Drug Store Products, Inc.
    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:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    10-19-2015
    End Marketing 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
    29485-7963-330 POUCH in 1 BOX / 2 TABLET, FILM COATED in 1 POUCH

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 29485-7963-2?

    The NDC Packaged Code 29485-7963-2 is assigned to a package of 25 pouch in 1 box / 2 tablet, film coated in 1 pouch of Benadryl, a human over the counter drug labeled by Lil' Drug Store Products, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 29485-7963 included in the NDC Directory?

    Yes, Benadryl with product code 29485-7963 is active and included in the NDC Directory. The product was first marketed by Lil' Drug Store Products, Inc. on October 19, 2015.

    What is the 11-digit format for NDC 29485-7963-2?

    The 11-digit format is 29485796302. 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 5-4-1 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
    5-4-129485-7963-25-4-229485-7963-02