45984-0003 NDC - NEOBRYXOL ULTRA ()

Drug Information

Product NDC: 45984-0003

Proprietary Name: Neobryxol Ultra

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Bryomed Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/4/2012

Package Information

No. Package Code Package Description Billing Unit
145984-0003-160 mL in 1 BOTTLE, DROPPER (45984-0003-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC45984-0003The 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 NAMENeobryxol UltraThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/4/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBryomed Inc.Name 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