Cromolyn Sodium
NDC Package 70556-101-96

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Cromolyn Sodium is a medication used to treat certain allergic eye conditions (vernal keratoconjunctivitis, vernal conjunctivitis, vernal keratitis). Marketed by Ailex Pharmaceuticals, Llc, this product is identified by NDC 70556-101 and is authorized under FDA application ANDA209264.

Identification & Billing

NDC Package Code
70556-101-96
Package Description
12 POUCH in 1 CARTON / 8 AMPULE in 1 POUCH / 5 mL in 1 AMPULE
Product Code
70556-101
11-Digit Billing Format
70556010196
RxNorm Crosswalk
  • RxCUI: 831261 - cromolyn sodium 100 MG in 5 mL Concentrate for Oral Solution
  • RxCUI: 831261 - cromolyn sodium 20 MG/ML Oral Solution
  • RxCUI: 831261 - cromolyn sodium 100 MG per 5 ML Concentrate for Oral Solution

Clinical Specifications

Proprietary Name
Cromolyn Sodium
Dosage Form
-
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.

Regulatory & Marketing

Labeler Name
Ailex Pharmaceuticals, Llc
FDA Application #
ANDA209264
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
10-16-2017
Listing Expiration
12-31-2021
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 70556-101-96 identifies a specific commercial package of 12 pouch in 1 carton / 8 ampule in 1 pouch / 5 ml in 1 ampule of Cromolyn Sodium, labeled by Ailex Pharmaceuticals, Llc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Ailex Pharmaceuticals, Llc on October 16, 2017. The current certification is valid through December 31, 2021.

What are the primary indications for this medication?

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.

How is this Ailex Pharmaceuticals, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70556010196. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
70556-101-96
11-Digit CMS (5-4-2)
70556-0101-96

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.