33992-6110 NDC - MULTI SYMPTOM DAYTIME ()

Drug Information

Product NDC: 33992-6110

Proprietary Name: Multi Symptom Daytime

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Greenbrier International, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/18/2018

Package Information

No. Package Code Package Description Billing Unit
133992-6110-11 BLISTER PACK in 1 CARTON (33992-6110-1) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Record

Field Name Field Value Definition
PRODUCT NDC33992-6110The 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 NAMEMulti Symptom DaytimeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/18/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGreenbrier International, Inc.Name 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