NDC 63981-453 Suphedrine Pe

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:
63981-453
Proprietary Name:
Suphedrine Pe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Costco Wholesale Corporation
Labeler Code:
63981
Start Marketing Date: [9]
12-06-2004
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
Shape:
ROUND (C48348)
Size(s):
6 MM
Imprint(s):
44;453
Score:
1

Product Packages

NDC Code 63981-453-69

Package Description: 1 BLISTER PACK in 1 CARTON / 144 TABLET, FILM COATED in 1 BLISTER PACK

Product Details

What is NDC 63981-453?

The NDC code 63981-453 is assigned by the FDA to the product Suphedrine Pe which is product labeled by Costco Wholesale Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63981-453-69 1 blister pack in 1 carton / 144 tablet, film coated 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 Suphedrine Pe?

Adults and children 12 years and over: 1 tablet every 4 hours. Do not take more than 6 tablets in 24 hours.  children under 12 years: do not use this product in children under 12 years of age

Which are Suphedrine Pe UNII Codes?

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

Which are Suphedrine Pe 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 Suphedrine Pe?

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 indicates multiple concept unique identifiers (RXCUIs) are 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".