46084-121 NDC - DAYTIME NIGHTTIME COLD/FLU RELIEF ()

Drug Information

Product NDC: 46084-121

Proprietary Name: DAYTIME NIGHTTIME COLD/FLU RELIEF

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: A P J Laboratories Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/1/2013

Package Information

No. Package Code Package Description Billing Unit
146084-121-011 KIT in 1 PACKAGE (46084-121-01) * 20 TABLET in 1 BLISTER PACK (46084-122-20) * 20 TABLET in 1 BLISTER PACK (46084-123-20)

NDC Record

Field Name Field Value Definition
PRODUCT NDC46084-121The 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 NAMEDAYTIME NIGHTTIME COLD/FLU RELIEFThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXA P JA 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 DATE6/1/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEA P J Laboratories LimitedName 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