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  5. NDC Package Code: 73629-001-22 Diphenhydramine Hydrochloride 50mg

NDC Package 73629-001-22 Diphenhydramine Hydrochloride 50mg

Capsule, Liquid Filled Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
73629-001-22
Package Description:
220 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product Code:
73629-001
Proprietary Name:
Diphenhydramine Hydrochloride 50mg
Non-Proprietary Name:
Diphenhydramine Hydrochloride 50mg
Substance Name:
Diphenhydramine Hydrochloride
Usage Information:
For relied of occasional sleeplessness
11-Digit NDC Billing Format:
73629000122
NDC to RxNorm Crosswalk:
  • RxCUI: 1020477 - diphenhydrAMINE HCl 50 MG Oral Capsule
  • RxCUI: 1020477 - diphenhydramine hydrochloride 50 MG Oral Capsule
  • RxCUI: 1020477 - diphenhydramine HCl 50 MG Oral Capsule
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Amz789 Llc
    Dosage Form:
    Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • DIPHENHYDRAMINE HYDROCHLORIDE 50 mg/1
    • Pharmacologic Class(es):
  • Histamine H1 Receptor Antagonists - [MoA] (Mechanism of Action)
  • Histamine-1 Receptor Antagonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    part338
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    09-21-2020
    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 73629-001-22?

    The NDC Packaged Code 73629-001-22 is assigned to a package of 220 capsule, liquid filled in 1 bottle of Diphenhydramine Hydrochloride 50mg, a human over the counter drug labeled by Amz789 Llc. The product's dosage form is capsule, liquid filled and is administered via oral form.

    Is NDC 73629-001 included in the NDC Directory?

    Yes, Diphenhydramine Hydrochloride 50mg with product code 73629-001 is active and included in the NDC Directory. The product was first marketed by Amz789 Llc on September 21, 2020 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 73629-001-22?

    The 11-digit format is 73629000122. 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
    5-3-273629-001-225-4-273629-0001-22