NDC Package 51148-007-01 Rabeprazole Sodium Tablets

Tablet, Delayed Release - View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
51148-007-01
Package Description:
1 BAG in 1 DRUM / 100000 TABLET, DELAYED RELEASE in 1 BAG
Product Code:
Non-Proprietary Name:
Rabeprazole Sodium Tablets
Substance Name:
Rabeprazole Sodium
Usage Information:
Rabeprazole 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. Rabeprazole belongs to a class of drugs known as proton pump inhibitors (PPIs).
11-Digit NDC Billing Format:
51148000701
Product Type:
Drug For Further Processing
Labeler Name:
Bushu Pharmaceuticals, Ltd.
Dosage Form:
Tablet, Delayed Release - A solid dosage form which releases a drug (or drugs) at a time other than promptly after administration. Enteric-coated articles are delayed release dosage forms.
Active Ingredient(s):
Sample Package:
N/A
Marketing Category:
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date:
08-19-1999
Listing Expiration Date:
12-31-2024
Exclude Flag:
N
Unfinished Product:
Yes
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.

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Frequently Asked Questions

What is NDC 51148-007-01?

The NDC Packaged Code 51148-007-01 is assigned to an UNFINISHED drug package of 1 bag in 1 drum / 100000 tablet, delayed release in 1 bag of Rabeprazole Sodium Tablets, drug for further processing labeled by Bushu Pharmaceuticals, Ltd.. The product's dosage form is tablet, delayed release and is administered via form.

Is NDC 51148-007 included in the NDC Directory?

Yes, Rabeprazole Sodium Tablets is an UNFINISHED PRODUCT with code 51148-007 that is active and included in the NDC Directory. The product was first marketed by Bushu Pharmaceuticals, Ltd. on August 19, 1999 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 51148-007-01?

The 11-digit format is 51148000701. 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
5-3-251148-007-015-4-251148-0007-01