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  5. NDC Package Code: 51662-1219-1 Diphenhydramine Hydrochloride

NDC Package 51662-1219-1 Diphenhydramine Hydrochloride

Injection Intramuscular; Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. Other Packages
    4. 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:
51662-1219-1
Package Description:
1 mL in 1 VIAL
Product Code:
51662-1219
Proprietary Name:
Diphenhydramine Hydrochloride
Non-Proprietary Name:
Diphenhydramine Hydrochloride
Substance Name:
Diphenhydramine Hydrochloride
Usage Information:
Diphenhydramine Hydrochloride Injection is effective in adults and pediatric patients, other than premature infants and neonates, for the following conditions when the oral form is impractical:AntihistaminicFor amelioration of allergic reactions to blood or plasma, in anaphylaxis as an adjunct to epinephrine and other standard measures after the acute symptoms have been controlled and for other uncomplicated allergic conditions of the immediate type when oral therapy is impossible or contraindicated.Motion SicknessFor active treatment of motion sickness.AntiparkinsonismFor use in parkinsonism, when oral therapy is impossible or contraindicated, as follows: parkinsonism in the elderly who are unable to tolerate more potent agents, mild cases of parkinsonism in other age groups and in other cases of parkinsonism in combination with centrally acting anticholinergic agents.
11-Digit NDC Billing Format:
51662121901
NDC to RxNorm Crosswalk:
  • RxCUI: 1723740 - diphenhydrAMINE HCl 50 MG in 1 ML Injection
  • RxCUI: 1723740 - 1 ML diphenhydramine hydrochloride 50 MG/ML Injection
  • RxCUI: 1723740 - diphenhydramine HCl 50 MG per 1 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hf Acquisition Co. Llc, Dba Health First
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • DIPHENHYDRAMINE HYDROCHLORIDE 50 mg/mL
    • 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:
    ANDA080817
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-16-2018
    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.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 51662-1219-1 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    51662121901J1200Diphenhydramine hcl injectio50 MG1111

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    51662-1219-325 POUCH in 1 CASE / 1 mL in 1 POUCH (51662-1219-2)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51662-1219-1?

    The NDC Packaged Code 51662-1219-1 is assigned to a package of 1 ml in 1 vial of Diphenhydramine Hydrochloride, a human prescription drug labeled by Hf Acquisition Co. Llc, Dba Health First. The product's dosage form is injection and is administered via intramuscular; intravenous form.

    Is NDC 51662-1219 included in the NDC Directory?

    Yes, Diphenhydramine Hydrochloride with product code 51662-1219 is active and included in the NDC Directory. The product was first marketed by Hf Acquisition Co. Llc, Dba Health First on August 16, 2018 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 51662-1219-1?

    The 11-digit format is 51662121901. 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
    5-4-151662-1219-15-4-251662-1219-01