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  5. NDC Package Code: 51662-1378-1 Atropine Sulfate

NDC Package 51662-1378-1 Atropine Sulfate

Injection Parenteral - 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:
51662-1378-1
Package Description:
1 SYRINGE in 1 BOX / 10 mL in 1 SYRINGE
Product Code:
51662-1378
Proprietary Name:
Atropine Sulfate
Non-Proprietary Name:
Atropine Sulfate
Substance Name:
Atropine Sulfate
Usage Information:
This medication is used before eye examinations (e.g., refraction) and to treat certain eye conditions (e.g., uveitis). It belongs to a class of drugs known as anticholinergics. Atropine works by widening (dilating) the pupil of the eye.
11-Digit NDC Billing Format:
51662137801
NDC to RxNorm Crosswalk:
  • RxCUI: 1190546 - atropine sulfate 1 MG in 10 ML Prefilled Syringe
  • RxCUI: 1190546 - 10 ML atropine sulfate 0.1 MG/ML Prefilled Syringe
  • RxCUI: 1190546 - atropine sulfate 1 MG per 10 ML Prefilled Syringe
    • 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):
  • Parenteral - Administration by injection, infusion, or implantation.
    • Active Ingredient(s):
  • ATROPINE SULFATE .1 mg/mL
    • Pharmacologic Class(es):
  • Anticholinergic - [EPC] (Established Pharmacologic Class)
  • Cholinergic Antagonists - [MoA] (Mechanism of Action)
  • Cholinergic Muscarinic Antagonist - [EPC] (Established Pharmacologic Class)
  • Cholinergic Muscarinic Antagonists - [MoA] (Mechanism of Action)
    • 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:
    10-15-2019
    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.

    Frequently Asked Questions

    What is NDC 51662-1378-1?

    The NDC Packaged Code 51662-1378-1 is assigned to a package of 1 syringe in 1 box / 10 ml in 1 syringe of Atropine Sulfate, a human prescription drug labeled by Hf Acquisition Co Llc, Dba Healthfirst. The product's dosage form is injection and is administered via parenteral form.

    Is NDC 51662-1378 included in the NDC Directory?

    Yes, Atropine Sulfate with product code 51662-1378 is active and included in the NDC Directory. The product was first marketed by Hf Acquisition Co Llc, Dba Healthfirst on October 15, 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 51662-1378-1?

    The 11-digit format is 51662137801. 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
    5-4-151662-1378-15-4-251662-1378-01