70692-108 NDC - ACETAMINOPHEN 500MG, DEXTROMETHORPHAN HBR 10MG, GUAIFENESIN 200MG, PHENYLEPHRINE HCL 5MG ()

Drug Information

Product NDC: 70692-108

Proprietary Name: Acetaminophen 500mg, Dextromethorphan HBr 10mg, Guaifenesin 200mg, Phenylephrine HCl 5mg

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name:	Strive Pharmaceuticals Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	12/20/2018

Package Information

No.	Package Code	Package Description	Billing Unit
1	70692-108-41	4 TABLET in 1 PACKAGE (70692-108-41)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	70692-108	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 500mg, Dextromethorphan HBr 10mg, Guaifenesin 200mg, Phenylephrine HCl 5mg	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	12/20/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Strive Pharmaceuticals Inc	Name of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Export to text format icon Download this NDC record in Text format: Export

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

Export to text format icon Download this NDC record in XML format: Export

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

« Previous Code

Next Code »