62192-8500 NDC - PREBOOST ()

Drug Information

Product NDC: 62192-8500

Proprietary Name: Preboost

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: 944 Corp
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/18/2014

Package Information

No. Package Code Package Description Billing Unit
162192-8500-110 PACKET in 1 BOX (62192-8500-1) / 1.2 mL in 1 PACKET

NDC Record

Field Name Field Value Definition
PRODUCT NDC62192-8500The 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 NAMEPreboostThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/18/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME944 CorpName 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