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  5. NDC Package Code: 51662-1218-1 Diphenhydramine Hci

NDC Package 51662-1218-1 Diphenhydramine Hci

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
51662-1218-1
Package Description:
1 mL in 1 CARTRIDGE
Product Code:
51662-1218
Proprietary Name:
Diphenhydramine Hci
Usage Information:
Diphenhydramine hydrochloride in the injectable form is effective in adults and pediatric patients, other than premature infants and neonates, for the following conditions when diphenhydramine hydrochloride in the oral form is impractical.Antihistaminic: For 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 sickness: For active treatment of motion sickness.Antiparkinsonism: For 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:
51662121801
NDC to RxNorm Crosswalk:
Labeler Name:
Hf Acquisition Co Llc, Dba Healthfirst
Sample Package:
No
FDA Application Number:
ANDA040140
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
11-19-2018
Listing Expiration Date:
12-31-2022
Exclude Flag:
I
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 51662-1218-1?

The NDC Packaged Code 51662-1218-1 is assigned to a package of 1 ml in 1 cartridge of Diphenhydramine Hci, labeled by Hf Acquisition Co Llc, Dba Healthfirst. The product's dosage form is and is administered via form.

Is NDC 51662-1218 included in the NDC Directory?

No, Diphenhydramine Hci with product code 51662-1218 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Hf Acquisition Co Llc, Dba Healthfirst on November 19, 2018 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 51662-1218-1?

The 11-digit format is 51662121801. 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
5-4-151662-1218-15-4-251662-1218-01