Prevymis Tablet, Film Coated
NDC Package 0006-3075-04

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

Package Information

Prevymis (letermovir) tablets is a medication used to prevent disease caused by a virus called cytomegalovirus (CMV) in people who have received a bone marrow transplant. This formulation utilizes a tablet, film coated delivery system. Marketed by Merck Sharp & Dohme Llc, this product is identified by NDC 0006-3075 and is authorized under FDA application NDA209939.

Identification & Billing

NDC Package Code
0006-3075-04
Package Description
14 BLISTER PACK in 1 CARTON / 1 TABLET, FILM COATED in 1 BLISTER PACK (0006-3075-03)
Product Code
11-Digit Billing Format
00006307504
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
14 EA
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Prevymis
Non-Proprietary Name
Letermovir
Substance Name
Letermovir
Dosage Form
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
This medication is used to prevent disease caused by a virus called cytomegalovirus (CMV) in people who have received a bone marrow transplant. CMV disease can lead to serious infections in the body, including an infection in the eye, called CMV retinitis, that can cause blindness. Letermovir is an anti-viral drug. It works by stopping the growth of the virus.

Regulatory & Marketing

Labeler Name
Merck Sharp & Dohme Llc
Product Type
Human Prescription Drug
FDA Application #
NDA209939
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
11-08-2017
Listing Expiration
12-31-2027
Exclude Flag
N
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (0006-3075). Click a package code to view its specific billing and regulatory data.

4 DOSE PACK in 1 CARTON / 7 TABLET, FILM COATED in 1 DOSE PACK (0006-3075-01)

* 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 0006-3075-04 identifies a specific commercial package of 14 blister pack in 1 carton / 1 tablet, film coated in 1 blister pack (0006-3075-03) of Prevymis, a human prescription drug labeled by Merck Sharp & Dohme Llc. This product is billed for "EA" each discreet unit and contains an estimated amount of 14 billable units per package. This tablet, film coated is formulated for oral use and contains letermovir as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Merck Sharp & Dohme Llc on November 08, 2017. The current certification is valid through December 31, 2027.

What are the primary indications for this medication?

This medication is used to prevent disease caused by a virus called cytomegalovirus (CMV) in people who have received a bone marrow transplant. CMV disease can lead to serious infections in the body, including an infection in the eye, called CMV retinitis, that can cause blindness. Letermovir is an anti-viral drug. It works by stopping the growth of the virus.

How is this Merck Sharp & Dohme Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00006307504. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 14 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 (4-4-2)
0006-3075-04
11-Digit CMS (5-4-2)
00006-3075-04

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