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Drug Information

Product NDC: 53002-3191

Proprietary Name: Guaifenesin and Codeine Phosphate

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: RPK Pharmaceuticals, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/1/2006

Package Information

No. Package Code Package Description Billing Unit
153002-3191-1118 mL in 1 BOTTLE (53002-3191-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC53002-3191The 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 NAMEGuaifenesin and Codeine PhosphateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/1/2006This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERPK Pharmaceuticals, 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