NDC Package 0179-1471-30 Famotidine

View Billable Units, 11-Digit Format, RxNorm

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:
0179-1471-30
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Famotidine
Usage Information:
Famotidine is used to treat ulcers of the stomach and intestines and to prevent intestinal ulcers 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. Famotidine belongs to a class of drugs known as H2 blockers. This medication is also available without a prescription. It is used to prevent and treat heartburn and other symptoms caused by too much acid in the stomach (acid indigestion). If you are taking this medication for self-treatment, it is important to read the manufacturer's package instructions carefully so you know when to consult your doctor or pharmacist.
11-Digit NDC Billing Format:
00179147130
Labeler Name:
Kaiser Foundation Hospitals
Sample Package:
No
FDA Application Number:
ANDA075511
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
02-16-2005
End Marketing Date:
03-31-2018
Listing Expiration Date:
03-31-2018
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
0179-1471-01100 TABLET, FILM COATED in 1 BOTTLE
0179-1471-5050 TABLET, FILM COATED in 1 BOTTLE
0179-1471-6060 TABLET, FILM COATED in 1 BOTTLE
0179-1471-9090 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0179-1471-30?

The NDC Packaged Code 0179-1471-30 is assigned to a package of 30 tablet, film coated in 1 bottle of Famotidine, labeled by Kaiser Foundation Hospitals. The product's dosage form is and is administered via form.

Is NDC 0179-1471 included in the NDC Directory?

No, Famotidine with product code 0179-1471 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Kaiser Foundation Hospitals on February 16, 2005 and its listing in the NDC Directory is set to expire on March 31, 2018 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0179-1471-30?

The 11-digit format is 00179147130. 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
4-4-20179-1471-305-4-200179-1471-30