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  5. NDC Package Code: 51662-1439-1 Physostigmine Salicylate

NDC Package 51662-1439-1 Physostigmine Salicylate

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
51662-1439-1
Package Description:
2 mL in 1 AMPULE
Product Code:
51662-1439
Proprietary Name:
Physostigmine Salicylate
Non-Proprietary Name:
Physostigmine Salicylate
Substance Name:
Physostigmine Salicylate
Usage Information:
To reverse the effect upon the central nervous system, caused by clinical or toxic dosages of drugs capable of producing the anticholinergic syndrome.
11-Digit NDC Billing Format:
51662143901
NDC to RxNorm Crosswalk:
  • RxCUI: 990982 - PHYSostigmine salicylate 1 MG/ML in 2 ML Injection
  • RxCUI: 990982 - 2 ML physostigmine salicylate 1 MG/ML Injection
  • RxCUI: 990982 - physostigmine salicylate 1 MG/ML per 2 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hf Acquisition Co Llc, Dba Healthfirst
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • PHYSOSTIGMINE SALICYLATE 1 mg/mL
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    12-22-2019
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    51662-1439-310 POUCH in 1 CASE / 1 AMPULE in 1 POUCH (51662-1439-2) / 2 mL in 1 AMPULE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51662-1439-1?

    The NDC Packaged Code 51662-1439-1 is assigned to a package of 2 ml in 1 ampule of Physostigmine Salicylate, a human prescription drug labeled by Hf Acquisition Co Llc, Dba Healthfirst. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 51662-1439 included in the NDC Directory?

    Yes, Physostigmine Salicylate with product code 51662-1439 is active and included in the NDC Directory. The product was first marketed by Hf Acquisition Co Llc, Dba Healthfirst on December 22, 2019 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 51662-1439-1?

    The 11-digit format is 51662143901. 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
    5-4-151662-1439-15-4-251662-1439-01