NDC Package 0404-9990-20 Atropine Sulfate

Atropine Sulfate Injection Injection Endotracheal; Intramedullary; Intramuscular; - View Billable Units, 11-Digit Format, RxNorm

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:
Package Description:
1 PACKAGE in 1 BAG / 20 mL in 1 PACKAGE
Product Code:
Proprietary Name:
Atropine Sulfate
Non-Proprietary Name:
Atropine Sulfate Injection
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:
NDC to RxNorm Crosswalk:
  • RxCUI: 1190776 - atropine sulfate 0.4 MG/ML Injectable Solution
  • RxCUI: 1190776 - atropine sulfate 1 MG per 2.5 ML Injectable Solution
  • RxCUI: 1190776 - atropine sulfate 1.2 MG per 3 ML Injectable Solution
  • RxCUI: 1190776 - atropine sulfate 2 MG per 5 ML Injectable Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Henry Schein, Inc.
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Endotracheal - Administration directly into the trachea.
  • Intramedullary - Administration within the marrow cavity of a bone.
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
  • Active Ingredient(s):
    Sample Package:
    FDA Application Number:
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    Listing Expiration Date:
    Exclude Flag:
    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.

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    Frequently Asked Questions

    What is NDC 0404-9990-20?

    The NDC Packaged Code 0404-9990-20 is assigned to a package of 1 package in 1 bag / 20 ml in 1 package of Atropine Sulfate, a human prescription drug labeled by Henry Schein, Inc.. The product's dosage form is injection and is administered via endotracheal; intramedullary; intramuscular; intravenous; subcutaneous form.

    Is NDC 0404-9990 included in the NDC Directory?

    Yes, Atropine Sulfate with product code 0404-9990 is active and included in the NDC Directory. The product was first marketed by Henry Schein, Inc. on December 21, 2022 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 0404-9990-20?

    The 11-digit format is 00404999020. 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 4-4-2 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