Fluorouracil Injection, Solution
NDC Package 46708-751-50

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

Package Information

Fluorouracil injection is fluorouracil is used to treat various types of cancer. This formulation utilizes a injection, solution delivery system. Marketed by Alembic Pharmaceuticals Limited, this product is identified by NDC 46708-751 and is authorized under FDA application ANDA217295.

Identification & Billing

NDC Package Code
46708-751-50
Package Description
1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON / 50 mL in 1 VIAL, PHARMACY BULK PACKAGE
Product Code
46708-751
11-Digit Billing Format
46708075150
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Fluorouracil
Non-Proprietary Name
Fluorouracil
Substance Name
Fluorouracil
Dosage Form
Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
Administration Route
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
FLUOROURACIL 50 mg/mL
Pharmacologic Class
Usage Information
Fluorouracil is used to treat various types of cancer. It is a chemotherapy drug that is used to slow or stop cancer cell growth. You should be tested for a DPD enzyme deficiency before you start treatment with fluorouracil. Ask your doctor for more details.

Regulatory & Marketing

Labeler Name
Alembic Pharmaceuticals Limited
Product Type
Human Prescription Drug
FDA Application #
ANDA217295
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
03-03-2023
Listing Expiration
12-31-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 46708-751-50 identifies a specific commercial package of 1 vial, pharmacy bulk package in 1 carton / 50 ml in 1 vial, pharmacy bulk package of Fluorouracil, a human prescription drug labeled by Alembic Pharmaceuticals Limited. This injection, solution is formulated for intravenous use and contains fluorouracil 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 Alembic Pharmaceuticals Limited on March 03, 2023. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

Fluorouracil is used to treat various types of cancer. It is a chemotherapy drug that is used to slow or stop cancer cell growth. You should be tested for a DPD enzyme deficiency before you start treatment with fluorouracil. Ask your doctor for more details.

How is this Alembic Pharmaceuticals Limited product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 46708075150. 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)
46708-751-50
11-Digit CMS (5-4-2)
46708-0751-50

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