57344-119 NDC - ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE ()

Drug Information

Product NDC: 57344-119

Proprietary Name: Acetaminophen, Guaifenesin, Phenylephrine Hydrochloride

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description	Billing Unit
1	57344-119-02	2 BLISTER PACK in 1 CARTON (57344-119-02) / 12 TABLET, COATED in 1 BLISTER PACK
2	57344-119-05	2 BLISTER PACK in 1 CARTON (57344-119-05) / 12 TABLET, COATED in 1 BLISTER PACK

Field Name	Field Value	Definition
PRODUCT NDC	57344-119	The 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 NAME	Acetaminophen, Guaifenesin, Phenylephrine Hydrochloride	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	12/28/2012	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	AAA Pharmaceutical, 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