NDC Package 76413-317-30 Zantac

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
76413-317-30
Package Description:
3 BLISTER PACK in 1 CARTON / 10 TABLET, COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Zantac
Usage Information:
Ranitidine is used to treat ulcers of the stomach and intestines and prevent them from coming back after they have healed. This medication is also used to treat certain stomach and throat (esophagus) problems (such as erosive esophagitis, gastroesophageal reflux disease-GERD, Zollinger-Ellison syndrome). It works by decreasing the amount of acid your stomach makes. It relieves symptoms such as cough that doesn't go away, stomach pain, heartburn, and difficulty swallowing. Ranitidine belongs to a class of drugs known as H2 blockers. This form of ranitidine is given by injection and is used for short-term treatment of these conditions when you cannot take this medication by mouth. Your doctor should switch you to taking this medication by mouth when possible. This drug has been withdrawn from the US market due to problems with safety. A possible cancer-causing impurity has been found in some ranitidine products.
11-Digit NDC Billing Format:
76413031730
NDC to RxNorm Crosswalk:
  • RxCUI: 312773 - ranitidine 75 MG Oral Tablet
  • RxCUI: 312773 - ranitidine 75 MG (as ranitidine hydrochloride 84 MG) Oral Tablet
  • RxCUI: 827183 - Zantac 75 MG Oral Tablet
  • RxCUI: 827183 - ranitidine 75 MG Oral Tablet [Zantac]
  • RxCUI: 827183 - Zantac 75 75 MG Oral Tablet
  • Labeler Name:
    Central Texas Community Health Centers
    Sample Package:
    No
    Start Marketing Date:
    12-21-2006
    Listing Expiration Date:
    12-31-2019
    Exclude Flag:
    I
    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 76413-317-30?

    The NDC Packaged Code 76413-317-30 is assigned to a package of 3 blister pack in 1 carton / 10 tablet, coated in 1 blister pack of Zantac, labeled by Central Texas Community Health Centers. The product's dosage form is and is administered via form.

    Is NDC 76413-317 included in the NDC Directory?

    No, Zantac with product code 76413-317 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Central Texas Community Health Centers on December 21, 2006 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 76413-317-30?

    The 11-digit format is 76413031730. 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 5-3-2 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
    5-3-276413-317-305-4-276413-0317-30