NDC Package 64679-742-02 Ranitidine

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
Frequently Asked Questions

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:

64679-742-02

Package Description:

250 TABLET in 1 BOTTLE

Product Code:

64679-742

Proprietary Name:

Ranitidine

Usage Information:

Ranitidine Tablets are indicated in: Short-term treatment of active duodenal ulcer. Most patients heal within 4 weeks. Studies available to date have not assessed the safety of ranitidine in uncomplicated duodenal ulcer for periods of more than 8 weeks.Maintenance therapy for duodenal ulcer patients at reduced dosage after healing of acute ulcers. No placebo-controlled comparative studies have been carried out for periods of longer than 1 year.The treatment of pathological hypersecretory conditions (e.g., Zollinger-Ellison syndrome and systemic mastocytosis).Short-term treatment of active, benign gastric ulcer. Most patients heal within 6 weeks and the usefulness of further treatment has not been demonstrated. Studies available to date have not assessed the safety of ranitidine in uncomplicated, benign gastric ulcer for periods of more than 6 weeks.Maintenance therapy for gastric ulcer patients at reduced dosage after healing of acute ulcers. Placebo-controlled studies have been carried out for 1 year.Treatment of GERD. Symptomatic relief commonly occurs within 24 hours after starting therapy with ranitidine 150 mg twice daily.Treatment of endoscopically diagnosed erosive esophagitis. Symptomatic relief of heartburn commonly occurs within 24 hours of therapy initiation with ranitidine 150 mg 4 times daily.Maintenance of healing of erosive esophagitis. Placebo-controlled trials have been carried out for 48 weeks. Concomitant antacids should be given as needed for pain relief to patients with active duodenal ulcer; active, benign gastric ulcer; hypersecretory states; GERD; and erosive esophagitis.

11-Digit NDC Billing Format:

64679074202

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

250 EA

NDC to RxNorm Crosswalk:

RxCUI: 198191 - ranitidine 150 MG Oral Tablet

RxCUI: 198191 - ranitidine 150 MG (as ranitidine HCl 168 MG) Oral Tablet

RxCUI: 198193 - ranitidine 300 MG Oral Tablet

RxCUI: 198193 - ranitidine 300 MG (as ranitidine HCl 336 MG) Oral Tablet

Labeler Name:

Wockhardt Usa Llc.

Sample Package:

Start Marketing Date:

12-11-2009

Listing Expiration Date:

12-31-2019

Exclude Flag:

Code Structure:

64679 - Wockhardt Usa Llc.
- 64679-742 - Ranitidine
  - 64679-742-02 - 250 TABLET in 1 BOTTLE

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 Code	Package Description
64679-742-01	30 TABLET in 1 BOTTLE
64679-742-03	10 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
64679-742-04	100 TABLET in 1 BOTTLE
64679-742-08	3000 TABLET in 1 DRUM
64679-742-09	7500 TABLET in 1 DRUM

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 64679-742-02?

The NDC Packaged Code 64679-742-02 is assigned to a package of 250 tablet in 1 bottle of Ranitidine, labeled by Wockhardt Usa Llc.. The product's dosage form is and is administered via form.

Is NDC 64679-742 included in the NDC Directory?

No, Ranitidine with product code 64679-742 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Wockhardt Usa Llc. on December 11, 2009 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 NDC billing unit for package 64679-742-02?

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 250.

What is the 11-digit format for NDC 64679-742-02?

The 11-digit format is 64679074202. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	64679-742-02	5-4-2	64679-0742-02

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