62257-575 NDC - QS PLUS ()

Drug Information

Product NDC: 62257-575

Proprietary Name: QS Plus

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ABC Compounding Co., Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/30/2003

Package Information

No. Package Code Package Description Billing Unit
162257-575-101000 mL in 1 CARTRIDGE (62257-575-10)
262257-575-121000 mL in 1 BAG (62257-575-12)
362257-575-13800 mL in 1 BAG (62257-575-13)
462257-575-143785 mL in 1 BOTTLE, PLASTIC (62257-575-14)
562257-575-15946 mL in 1 BOTTLE, PLASTIC (62257-575-15)
662257-575-16236 mL in 1 BOTTLE, PLASTIC (62257-575-16)
762257-575-17532 mL in 1 BOTTLE, PLASTIC (62257-575-17)
862257-575-1850 mL in 1 BOTTLE, PLASTIC (62257-575-18)
962257-575-24115 mL in 1 BOTTLE, PLASTIC (62257-575-24)
1062257-575-55208200 mL in 1 DRUM (62257-575-55)

NDC Record

Field Name Field Value Definition
PRODUCT NDC62257-575The 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 NAMEQS PlusThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/30/2003This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEABC Compounding Co., 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: 11/18/2019