55315-531 NDC - EXTRA STRENGTH PAIN RELIEVER ()

Drug Information

Product NDC: 55315-531

Proprietary Name: Extra Strength Pain Reliever

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: FRED'S, INC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/11/2005

Package Information

No. Package Code Package Description Billing Unit
155315-531-121 BOTTLE in 1 CARTON (55315-531-12) / 100 TABLET in 1 BOTTLE
255315-531-571 BOTTLE in 1 CARTON (55315-531-57) / 125 TABLET in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC55315-531The 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 NAMEExtra Strength Pain RelieverThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/11/2005This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEFRED'S, 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