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  5. NDC Package Code: 0093-0507-93 Folic Acid

NDC Package 0093-0507-93 Folic Acid

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:
0093-0507-93
Package Description:
100 BLISTER PACK in 1 BOX / 1 TABLET in 1 BLISTER PACK (0093-0507-19)
Product Code:
0093-0507
Proprietary Name:
Folic Acid
Usage Information:
Folic acid is the man-made form of folate. Folate is a B-vitamin naturally found in some foods. It is needed to form healthy cells, especially red blood cells. Folic acid supplements may come in different forms (such as L-methylfolate, levomefolate, methyltetrahydrofolate). They are used to treat or prevent low folate levels. Low folate levels can lead to certain types of anemia. Conditions that can cause low folate levels include poor diet, pregnancy, alcoholism, liver disease, certain stomach/intestinal problems, kidney dialysis, among others. Women of childbearing age should receive adequate amounts of folic acid either through their diet or supplements to prevent infant spinal cord birth defects.
11-Digit NDC Billing Format:
00093050793
Labeler Name:
Teva Pharmaceuticals Usa Inc
Sample Package:
No
FDA Application Number:
ANDA080600
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
03-23-2010
End Marketing Date:
11-01-2011
Listing Expiration Date:
11-01-2011
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 0093-0507-93?

The NDC Packaged Code 0093-0507-93 is assigned to a package of 100 blister pack in 1 box / 1 tablet in 1 blister pack (0093-0507-19) of Folic Acid, labeled by Teva Pharmaceuticals Usa Inc. The product's dosage form is and is administered via form.

Is NDC 0093-0507 included in the NDC Directory?

No, Folic Acid with product code 0093-0507 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Teva Pharmaceuticals Usa Inc on March 23, 2010 and its listing in the NDC Directory is set to expire on November 01, 2011 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0093-0507-93?

The 11-digit format is 00093050793. 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
4-4-20093-0507-935-4-200093-0507-93