Hycamtin
NDC Package 0007-4201-01

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 discontinued by the firm.

Hycamtin is a medication used to treat small cell lung cancer. Marketed by Glaxosmithkline Llc, this product is identified by NDC 0007-4201 and is authorized under FDA application NDA020671.

Identification & Billing

NDC Package Code
0007-4201-01
Package Description
1 VIAL in 1 PACKAGE / 4 mL in 1 VIAL
Product Code
0007-4201
11-Digit Billing Format
00007420101
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
1 EA

Clinical Specifications

Proprietary Name
Hycamtin
Dosage Form
-
Usage Information
This medication is used to treat small cell lung cancer. It works by killing cancer cells or slowing their growth.

Regulatory & Marketing

Labeler Name
Glaxosmithkline Llc
FDA Application #
NDA020671
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
06-07-1996
End Marketing Date
07-31-2018
Listing Expiration
07-31-2018
Exclude Flag
D
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 0007-4201-01 identifies a specific commercial package of 1 vial in 1 package / 4 ml in 1 vial of Hycamtin, labeled by Glaxosmithkline Llc. This product is billed for "EA" each discreet unit and contains an estimated amount of 1 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 Glaxosmithkline Llc on June 07, 1996. The current certification is valid through July 31, 2018.

What are the primary indications for this medication?

This medication is used to treat small cell lung cancer. It works by killing cancer cells or slowing their growth.

How is this Glaxosmithkline Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00007420101. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1 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)
0007-4201-01
11-Digit CMS (5-4-2)
00007-4201-01

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