NDC Package 50090-1202-0 Cromolyn Sodium

Solution/ Drops Ophthalmic - 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:
50090-1202-0
Package Description:
10 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Cromolyn Sodium
Non-Proprietary Name:
Cromolyn Sodium
Substance Name:
Cromolyn Sodium
Usage Information:
This medication is used to treat certain allergic eye conditions (vernal keratoconjunctivitis, vernal conjunctivitis, vernal keratitis). It prevents itching of the eyes that can occur with these conditions. Cromolyn is known as a mast cell stabilizer. It works by blocking certain natural substances (histamine, SRS-A) that cause allergic symptoms.
11-Digit NDC Billing Format:
50090120200
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
10 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 831109 - cromolyn sodium 4 % Ophthalmic Solution
  • RxCUI: 831109 - cromolyn sodium 40 MG/ML Ophthalmic Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    A-s Medication Solutions
    Dosage Form:
    Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA075282
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-29-1999
    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 50090-1202-0?

    The NDC Packaged Code 50090-1202-0 is assigned to a package of 10 ml in 1 bottle, plastic of Cromolyn Sodium, a human prescription drug labeled by A-s Medication Solutions. The product's dosage form is solution/ drops and is administered via ophthalmic form.This product is billed per "ML" milliliter and contains an estimated amount of 10 billable units per package.

    Is NDC 50090-1202 included in the NDC Directory?

    Yes, Cromolyn Sodium with product code 50090-1202 is active and included in the NDC Directory. The product was first marketed by A-s Medication Solutions on June 29, 1999 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 NDC billing unit for package 50090-1202-0?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 10.

    What is the 11-digit format for NDC 50090-1202-0?

    The 11-digit format is 50090120200. 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
    5-4-150090-1202-05-4-250090-1202-00