Acid Reducer Powder Powder, For Suspension
NDC Package 75907-237-42

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Acid Reducer Powder (omeprazole and sodium bicarbonate) powders is for adults 18 years of age and older: this product is to be used once a day (every 24 hours), every day for 14 days it may take 1 to 4 days for full effect, although some people get complete relief of symptoms within 24 hours 14-Day Course of Treatmentproduct should be taken at least 1 hour before eating in the morning take every day for 14 days do not take more than once a day empty packet contents into a small cup containing 2 tablespoons of WATERDO NOT USE WITH OTHER LIQUIDS OR FOOD stir well and drink immediately refill cup with water and drink do not use for more than 14 days unless directed by your doctorRepeated 14-Day Courses (if needed)you may repeat a 14-day course every 4 months do not take for more than 14 days or more often than every 4 months unless directed by a doctor children under 18 years of age: ask a doctor. This formulation utilizes a powder, for suspension delivery system. Marketed by Dr. Reddy's Laboratories Inc.,, this product is identified by NDC 75907-237 and is authorized under FDA application ANDA217784.

Identification & Billing

NDC Package Code
75907-237-42
Package Description
42 PACKET in 1 CARTON / 1 POWDER, FOR SUSPENSION in 1 PACKET
Product Code
75907-237
11-Digit Billing Format
75907023742
RxNorm Crosswalk
  • RxCUI: 753562 - omeprazole 20 MG / sodium bicarbonate 1680 MG Powder for Oral Suspension
  • RxCUI: 753562 - Omeprazole 20 MG / NaHCO3 1680 MG Powder for Oral Suspension

Clinical Specifications

Proprietary Name
Acid Reducer Powder
Non-Proprietary Name
Omeprazole And Sodium Bicarbonate
Substance Name
Omeprazole; Sodium Bicarbonate
Dosage Form
Powder, For Suspension - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a suspension (a liquid preparation containing the solid particles dispersed in the liquid vehicle).
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
For adults 18 years of age and older: this product is to be used once a day (every 24 hours), every day for 14 days it may take 1 to 4 days for full effect, although some people get complete relief of symptoms within 24 hours 14-Day Course of Treatmentproduct should be taken at least 1 hour before eating in the morning take every day for 14 days do not take more than once a day empty packet contents into a small cup containing 2 tablespoons of WATERDO NOT USE WITH OTHER LIQUIDS OR FOOD stir well and drink immediately refill cup with water and drink do not use for more than 14 days unless directed by your doctorRepeated 14-Day Courses (if needed)you may repeat a 14-day course every 4 months do not take for more than 14 days or more often than every 4 months unless directed by a doctor children under 18 years of age: ask a doctor. Heartburn in children may sometimes be caused by a serious condition.

Regulatory & Marketing

Labeler Name
Dr. Reddy's Laboratories Inc.,
Product Type
Human Otc Drug
FDA Application #
ANDA217784
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
07-15-2024
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (75907-237). Click a package code to view its specific billing and regulatory data.

75907-237-14
14 PACKET in 1 CARTON / 1 POWDER, FOR SUSPENSION in 1 PACKET

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 75907-237-42 identifies a specific commercial package of 42 packet in 1 carton / 1 powder, for suspension in 1 packet of Acid Reducer Powder, a human over the counter drug labeled by Dr. Reddy's Laboratories Inc.,. This powder, for suspension is formulated for oral use and contains omeprazole; sodium bicarbonate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Dr. Reddy's Laboratories Inc., on July 15, 2024. The current certification is valid through December 31, 2026.

How is this Dr. Reddy's Laboratories Inc., product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 75907023742. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
75907-237-42
11-Digit CMS (5-4-2)
75907-0237-42

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.