55992-717 NDC - NAIL MD ()

Drug Information

Product NDC: 55992-717

Proprietary Name: Nail MD

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: OMG Medical Group, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/14/2013

Package Information

No. Package Code Package Description Billing Unit
155992-717-01100 mg in 1 PACKAGE (55992-717-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55992-717The 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 NAMENail MDThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/14/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEOMG Medical Group, LLCName 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