Shoprite Antacid
NDC Package 41190-357-40
Package Information
Shoprite Antacid is a . Marketed by Wakefern Food Corporation, this product is identified by NDC 41190-357 and is authorized under FDA application part331.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 41190 - Wakefern Food Corporation
- 41190-357 - Shoprite Antacid
- 41190-357-40 - 355 mL in 1 BOTTLE
- 41190-357 - Shoprite Antacid
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 the distribution configuration for this product package?
The code 41190-357-40 identifies a specific commercial package of 355 ml in 1 bottle of Shoprite Antacid, labeled by Wakefern Food Corporation. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Wakefern Food Corporation on August 28, 2013. The current certification is valid through January 31, 2020.
How is this Wakefern Food Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 41190035740. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.