NDC Package 16714-362-04 Famotidine

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory .

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:
16714-362-04
Package Description:
100 TABLET 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:
16714036204
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
Labeler Name:
Northstar Rxllc
Sample Package:
No
FDA Application Number:
ANDA078916
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
07-01-2009
End Marketing Date:
11-30-2015
Listing Expiration Date:
11-30-2015
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
16714-362-0130 TABLET in 1 BOTTLE
16714-362-0260 TABLET in 1 BOTTLE
16714-362-0390 TABLET in 1 BOTTLE
16714-362-05500 TABLET in 1 BOTTLE
16714-362-061000 TABLET in 1 BOTTLE
16714-362-11100 TABLET in 1 CARTON

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 16714-362-04?

The NDC Packaged Code 16714-362-04 is assigned to a package of 100 tablet in 1 bottle of Famotidine, labeled by Northstar Rxllc. The product's dosage form is and is administered via form.

Is NDC 16714-362 included in the NDC Directory?

The product was first marketed by Northstar Rxllc on July 01, 2009 and its listing in the NDC Directory is set to expire on November 30, 2015 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 16714-362-04?

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 100.

What is the 11-digit format for NDC 16714-362-04?

The 11-digit format is 16714036204. 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
5-3-216714-362-045-4-216714-0362-04