NDC Package 70556-102-60 Cromolyn Sodium

Solution Intrabronchial - 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:
70556-102-60
Package Description:
2 POUCH in 1 CARTON / 30 VIAL, SINGLE-DOSE in 1 POUCH (70556-102-30) / 2 mL in 1 VIAL, SINGLE-DOSE
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:
70556010260
NDC to RxNorm Crosswalk:
  • RxCUI: 831246 - cromolyn sodium 20 MG in 2 ML Inhalation Solution
  • RxCUI: 831246 - cromolyn sodium 10 MG/ML Inhalation Solution
  • RxCUI: 831246 - cromolyn sodium 20 MG per 2 ML Inhalation Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Ailex Pharmaceuticals, Llc
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Intrabronchial - Administration within a bronchus.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA209453
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-24-2017
    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 70556-102-60?

    The NDC Packaged Code 70556-102-60 is assigned to a package of 2 pouch in 1 carton / 30 vial, single-dose in 1 pouch (70556-102-30) / 2 ml in 1 vial, single-dose of Cromolyn Sodium, a human prescription drug labeled by Ailex Pharmaceuticals, Llc. The product's dosage form is solution and is administered via intrabronchial form.

    Is NDC 70556-102 included in the NDC Directory?

    Yes, Cromolyn Sodium with product code 70556-102 is active and included in the NDC Directory. The product was first marketed by Ailex Pharmaceuticals, Llc on October 24, 2017 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 70556-102-60?

    The 11-digit format is 70556010260. 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 5-3-2 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
    5-3-270556-102-605-4-270556-0102-60