16571-302 NDC - GUAIFENESIN AC ()

Drug Information

Product NDC: 16571-302

Proprietary Name: Guaifenesin AC

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description	Billing Unit
1	16571-302-16	473 mL in 1 BOTTLE (16571-302-16)	ML

Field Name	Field Value	Definition
PRODUCT NDC	16571-302	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	Guaifenesin AC	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	3/1/2015	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Rising Pharmaceuticals	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