Neomed Pharmaceutical
NDC Package 70898-102-12

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.

Neomed Pharmaceutical is hydrocortisone suppositories are indicated for use in:inflamed hemorrhoidspost-irradiation (factitial) proctitisas an adjunct in the treatment of chronic ulcerative colitiscryptitisother inflammatory conditions of anorectum and pruritus ani. Marketed by Neomed Pharmaceutical, this product is identified by NDC 70898-102.

Identification & Billing

NDC Package Code
70898-102-12
Package Description
12 SUPPOSITORY in 1 BOX
Product Code
70898-102
11-Digit Billing Format
70898010212
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
12 EA
RxNorm Crosswalk
RxCUI: 1291082 - hydrocortisone acetate 25 MG Rectal Suppository

Clinical Specifications

Proprietary Name
Neomed Pharmaceutical
Dosage Form
-
Usage Information
Hydrocortisone suppositories are indicated for use in:inflamed hemorrhoidspost-irradiation (factitial) proctitisas an adjunct in the treatment of chronic ulcerative colitiscryptitisother inflammatory conditions of anorectum and pruritus ani.

Regulatory & Marketing

Labeler Name
Neomed Pharmaceutical
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
03-05-2018
Listing Expiration
12-31-2019
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 70898-102-12 identifies a specific commercial package of 12 suppository in 1 box of Neomed Pharmaceutical, labeled by Neomed Pharmaceutical. This product is billed for "EA" each discreet unit and contains an estimated amount of 12 billable units per package. 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 Neomed Pharmaceutical on March 05, 2018. The current certification is valid through December 31, 2019.

How is this Neomed Pharmaceutical product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70898010212. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 12 total billable units per package. 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)
70898-102-12
11-Digit CMS (5-4-2)
70898-0102-12

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