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70112-150 NDC - LEVIGOLT ()

Drug Information

Product NDC: 70112-150

Proprietary Name: LevigoLT

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Topicare Management, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/9/2017

Package Information

No. Package Code Package Description Billing Unit
170112-150-011 TUBE in 1 CARTON (70112-150-01) / 76.5 g in 1 TUBEGM

NDC Record

Field Name Field Value Definition
PRODUCT NDC70112-150The 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 NAMELevigoLTThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/9/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMETopicare Management, 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