49035-103 NDC - EQUATE ULTRA STRENGTH ANTACID CALCIUM CARBONATE ()

Drug Information

Product NDC: 49035-103

Proprietary Name: equate Ultra Strength Antacid Calcium Carbonate

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Wal-Mart Stores,Inc.,
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/20/2015

Package Information

No. Package Code Package Description Billing Unit
149035-103-021 BOTTLE, PLASTIC in 1 PACKAGE (49035-103-02) / 30 mL in 1 BOTTLE, PLASTIC (49035-103-01)
249035-103-1372 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (49035-103-13)
349035-103-37160 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (49035-103-37)

NDC Record

Field Name Field Value Definition
PRODUCT NDC49035-103The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEequate Ultra Strength Antacid Calcium CarbonateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXAssorted FruitA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE9/16/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWal-Mart Stores,Inc.,Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC49035-103The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEExotic Cherry Hand SanitizerThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXbodycologyA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE5/20/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWal-Mart Stores IncName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC49035-103The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEequate Ultra Strength Antacid Calcium CarbonateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXTropical FruitA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE10/20/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWal-Mart Stores,Inc.,Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023