NDC Package 0135-0096-26 Gaviscon Regular Strength

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:
0135-0096-26
Package Description:
100 TABLET, CHEWABLE in 1 BOTTLE
Product Code:
Proprietary Name:
Gaviscon Regular Strength
Usage Information:
This medication is used to treat the symptoms of too much stomach acid such as stomach upset, heartburn, and acid indigestion. Aluminum and magnesium antacids work quickly to lower the acid in the stomach. Liquid antacids usually work faster/better than tablets or capsules. This medication works only on existing acid in the stomach. It does not prevent acid production. It may be used alone or with other medications that lower acid production (including H2 blockers such as cimetidine/ranitidine and proton pump inhibitors such as omeprazole).
11-Digit NDC Billing Format:
00135009626
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 212978 - Gaviscon Extra Strength 160 MG / 105 MG Chewable Tablet
  • RxCUI: 212978 - aluminum hydroxide 160 MG / magnesium carbonate 105 MG Chewable Tablet [Gaviscon]
  • RxCUI: 212978 - Gaviscon Extra Strength (aluminum hydroxide 160 MG / magnesium carbonate 105 MG) Chewable Tablet
  • RxCUI: 308072 - aluminum hydroxide 160 MG / magnesium carbonate 105 MG Chewable Tablet
Labeler Name:
Haleon Us Holdings Llc
Sample Package:
No
FDA Application Number:
M001
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
06-13-2011
End Marketing Date:
06-11-2025
Listing Expiration Date:
06-11-2025
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.

Frequently Asked Questions

What is NDC 0135-0096-26?

The NDC Packaged Code 0135-0096-26 is assigned to a package of 100 tablet, chewable in 1 bottle of Gaviscon Regular Strength, labeled by Haleon Us Holdings Llc. The product's dosage form is and is administered via form.

Is NDC 0135-0096 included in the NDC Directory?

No, Gaviscon Regular Strength with product code 0135-0096 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Haleon Us Holdings Llc on June 13, 2011 and its listing in the NDC Directory is set to expire on June 11, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0135-0096-26?

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 0135-0096-26?

The 11-digit format is 00135009626. 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
4-4-20135-0096-265-4-200135-0096-26