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  5. NDC Package Code: 0093-0670-05 Gemfibrozil

NDC Package 0093-0670-05 Gemfibrozil

View Billable Units, 11-Digit Format, RxNorm

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.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0093-0670-05
Package Description:
500 TABLET, FILM COATED in 1 BOTTLE
Product Code:
0093-0670
Proprietary Name:
Gemfibrozil
Usage Information:
Gemfibrozil is used along with a proper diet to help lower fats (triglycerides) and raise "good" cholesterol (HDL) in the blood. It may also help to lower "bad" cholesterol (LDL). Gemfibrozil belongs to a group of drugs known as "fibrates." It works by decreasing the amount of fat produced by the liver. Lowering triglycerides in people with very high triglyceride blood levels may decrease the risk of pancreas disease (pancreatitis). However, gemfibrozil might not lower your risk of a heart attack or stroke. Talk to your doctor about the risk and benefits of gemfibrozil. In addition to eating a proper diet (such as a low-cholesterol/low-fat diet), other lifestyle changes that may help this medication work better include exercising, drinking less alcohol, losing weight if overweight, and stopping smoking.
11-Digit NDC Billing Format:
00093067005
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
500 EA
Labeler Name:
Teva Pharmaceuticals Usa, Inc.
Sample Package:
No
FDA Application Number:
ANDA074256
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
11-24-1993
End Marketing Date:
03-31-2020
Listing Expiration Date:
03-31-2020
Exclude Flag:
D
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 0093-0670-05?

The NDC Packaged Code 0093-0670-05 is assigned to a package of 500 tablet, film coated in 1 bottle of Gemfibrozil, labeled by Teva Pharmaceuticals Usa, Inc.. The product's dosage form is and is administered via form.

Is NDC 0093-0670 included in the NDC Directory?

No, Gemfibrozil with product code 0093-0670 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Teva Pharmaceuticals Usa, Inc. on November 24, 1993 and its listing in the NDC Directory is set to expire on March 31, 2020 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0093-0670-05?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 500.

What is the 11-digit format for NDC 0093-0670-05?

The 11-digit format is 00093067005. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
4-4-20093-0670-055-4-200093-0670-05