10337-332 NDC - CUTIVATE ()

Drug Information

Product NDC: 10337-332

Proprietary Name: Cutivate

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: PharmaDerm a division of Fougera Pharmaceuticals Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/18/1990

Package Information

No. Package Code Package Description Billing Unit
110337-332-3030 g in 1 TUBE (10337-332-30)GM
210337-332-6060 g in 1 TUBE (10337-332-60)GM

NDC Record

Field Name Field Value Definition
PRODUCT NDC10337-332The 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 NAMECutivateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/18/1990This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEPharmaDerm a division of Fougera Pharmaceuticals 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