NDC 46084-021 Aprofen Regular Strength

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:
46084-021
Proprietary Name:
Aprofen Regular Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
A P J Laboratories Limited
Labeler Code:
46084
Start Marketing Date: [9]
02-21-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
10 MM
Imprint(s):
200MG
Score:
1

Product Packages

NDC Code 46084-021-22

Package Description: 50 TABLET in 1 BLISTER PACK

NDC Code 46084-021-23

Package Description: 100 TABLET in 1 BLISTER PACK

NDC Code 46084-021-24

Package Description: 250 TABLET in 1 BLISTER PACK

NDC Code 46084-021-26

Package Description: 500 TABLET in 1 BLISTER PACK

NDC Code 46084-021-31

Package Description: 2 TABLET in 1 BLISTER PACK

Product Details

What is NDC 46084-021?

The NDC code 46084-021 is assigned by the FDA to the product Aprofen Regular Strength which is product labeled by A P J Laboratories Limited. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 46084-021-22 50 tablet in 1 blister pack , 46084-021-23 100 tablet in 1 blister pack , 46084-021-24 250 tablet in 1 blister pack , 46084-021-26 500 tablet in 1 blister pack , 46084-021-31 2 tablet 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 Aprofen Regular Strength?

Temporarily relieves minor aches and pains due to:headachemuscular achesminor pain of arthritistoothachebackachethe common coldmenstrual crampstemporarily reduces fever

Which are Aprofen Regular Strength UNII Codes?

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

Which are Aprofen Regular Strength 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 Aprofen Regular Strength?

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".