61919-851 NDC - TRANSDERM-IQ ()

Drug Information

Product NDC: 61919-851

Proprietary Name: TRANSDERM-IQ

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Direct_Rx
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/25/2019

Package Information

No. Package Code Package Description Billing Unit
161919-851-04113 g in 1 TUBE (61919-851-04)GM

NDC Record

Field Name Field Value Definition
PRODUCT NDC61919-851The 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 NAMETRANSDERM-IQThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/25/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDirect_RxName 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