NDC Package 55315-019-14 Lansoprazole

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:
55315-019-14
Package Description:
1 BLISTER PACK in 1 BOX / 14 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Lansoprazole
Usage Information:
Lansoprazole is used to treat certain stomach and esophagus problems (such as acid reflux, ulcers). It works by decreasing the amount of acid your stomach makes. It relieves symptoms such as heartburn, difficulty swallowing, and persistent cough. This medication helps heal acid damage to the stomach and esophagus, helps prevent ulcers, and may help prevent cancer of the esophagus. Lansoprazole belongs to a class of drugs known as proton pump inhibitors (PPIs). If you are self-treating with this medication, over-the-counter lansoprazole products are used to treat frequent heartburn (occurring 2 or more days a week). Since it may take 1 to 4 days to have full effect, these products do not relieve heartburn right away. For over-the-counter products, carefully read the package instructions to make sure the product is right for you. Check the ingredients on the label even if you have used the product before. The manufacturer may have changed the ingredients. Also, products with similar brand names may contain different ingredients meant for different purposes. Taking the wrong product could harm you.
11-Digit NDC Billing Format:
55315001914
NDC to RxNorm Crosswalk:
  • RxCUI: 596843 - lansoprazole 15 MG Delayed Release Oral Capsule
  • Labeler Name:
    Freds Inc
    Sample Package:
    No
    Start Marketing Date:
    12-04-2012
    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 55315-019-14?

    The NDC Packaged Code 55315-019-14 is assigned to a package of 1 blister pack in 1 box / 14 capsule, delayed release in 1 blister pack of Lansoprazole, labeled by Freds Inc. The product's dosage form is and is administered via form.

    Is NDC 55315-019 included in the NDC Directory?

    No, Lansoprazole with product code 55315-019 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Freds Inc on December 04, 2012 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 55315-019-14?

    The 11-digit format is 55315001914. 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
    5-3-255315-019-145-4-255315-0019-14