Silace
NDC Package 17856-0116-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

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

Silace is take as indicated by doctor this product must be given in a 6 to 8 oz. Marketed by Atlantic Biologicals Corp., this product is identified by NDC 17856-0116 and is authorized under FDA application part334.

Identification & Billing

NDC Package Code
17856-0116-2
Package Description
25 mL in 1 CUP
Product Code
11-Digit Billing Format
17856011602
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Units Per Package
25 ML
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Silace
Dosage Form
-
Usage Information
Take as indicated by doctor this product must be given in a 6 to 8 oz. glass of milk or fruit juice or infant's formula to prevent throat irritation. Dose may be taken as a single daily dose or in divided doses dosage should be adjusted to individual responsehigher doses are recommended for initial therapythe effect on stools is usually apparent 1 to 3 days after the first doseAdults and children over 12 years50 to 200 mg (1 to 4 teaspoonful)Children 6 to under 12 years50 to 100 mg (1 to 2 teaspoonful) Children 3 to under 6 years25 to 50 mg(1/2 to 1 teaspoonful)Children under 3 years of ageAsk a doctor

Regulatory & Marketing

Labeler Name
Atlantic Biologicals Corp.
FDA Application #
part334
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
10-05-1990
Listing Expiration
12-31-2018
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 17856-0116-2 identifies a specific commercial package of 25 ml in 1 cup of Silace, labeled by Atlantic Biologicals Corp.. This product is billed per "ML" milliliter and contains an estimated amount of 25 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 Atlantic Biologicals Corp. on October 05, 1990. The current certification is valid through December 31, 2018.

How is this Atlantic Biologicals Corp. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 17856011602. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 25 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 (5-4-1)
17856-0116-2
11-Digit CMS (5-4-2)
17856-0116-02

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