71589-018 NDC - CLOBETASOL PROPIONATE ()

Drug Information

Product NDC: 71589-018

Proprietary Name: CLOBETASOL PROPIONATE

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Aleor Dermaceuticals Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	4/21/2022

No.	Package Code	Package Description	Billing Unit
1	71589-018-31	1 CAN in 1 CARTON (71589-018-31) / 100 g in 1 CAN
2	71589-018-50	1 CAN in 1 CARTON (71589-018-50) / 50 g in 1 CAN

Field Name	Field Value	Definition
PRODUCT NDC	71589-018	The 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 NAME	CLOBETASOL PROPIONATE	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	4/21/2022	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Aleor Dermaceuticals Limited	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 5/3/2024