51672-1296 NDC - DIFLORASONE DIACETATE ()

Drug Information

Product NDC: 51672-1296

Proprietary Name: Diflorasone Diacetate

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Taro Pharmaceuticals U.S.A., Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	4/24/2000

No.	Package Code	Package Description	Billing Unit
1	51672-1296-1	1 TUBE in 1 CARTON (51672-1296-1) / 15 g in 1 TUBE	GM
2	51672-1296-2	1 TUBE in 1 CARTON (51672-1296-2) / 30 g in 1 TUBE	GM
3	51672-1296-3	1 TUBE in 1 CARTON (51672-1296-3) / 60 g in 1 TUBE	GM

Field Name	Field Value	Definition
PRODUCT NDC	51672-1296	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	Diflorasone Diacetate	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	4/24/2000	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Taro Pharmaceuticals U.S.A., Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024