Search Icon

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):

Labeler Information

Labeler Name: Rising Pharmaceuticals
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/1/2015

Package Information

No. Package Code Package Description Billing Unit
116571-302-16473 mL in 1 BOTTLE (16571-302-16)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC16571-302The 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 ACThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/1/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERising PharmaceuticalsName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023