NDC 53217-058 Bismatrol

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
53217-058
Proprietary Name:
Bismatrol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
53217
Start Marketing Date: [9]
01-03-2003
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Shape:
ROUND (C48348)
Size(s):
17 MM
Imprint(s):
GDC122
Score:
1

Code Structure Chart

Product Details

What is NDC 53217-058?

The NDC code 53217-058 is assigned by the FDA to the product Bismatrol which is product labeled by Aidarex Pharmaceuticals Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53217-058-01 30 tablet, chewable in 1 blister pack . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Bismatrol?

Chew or dissolve in mouthadults and children 12 years and over: 2 tablets every 1/2 to 1 hour as neededdo not take more than 8 doses (16 tablets) in 24 hourschildren under 12 years: ask a doctordrink plenty of fluids to help prevent dehydration which may accompany diarrhea.Other information: each tablet contains:sodium less than 1 mgsalicylate 102 mgcalcium 140 mgvery low sodiumavoid excessive heat (over 104˚F or 40˚C)TAMPER EVIDENT: Do not use if individual compartments are torn or missing.

Which are Bismatrol UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Bismatrol Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Bismatrol?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".