42582-801 NDC - SODIUM SULFACETAMIDE 9.8%, SULFUR 4.8% ()

Drug Information

Product NDC: 42582-801

Proprietary Name: Sodium Sulfacetamide 9.8%, Sulfur 4.8%

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Bi-Coastal Pharma International LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	3/27/2017

No.	Package Code	Package Description	Billing Unit
1	42582-801-11	285 g in 1 BOTTLE (42582-801-11)	GM

Field Name	Field Value	Definition
PRODUCT NDC	42582-801	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	Sodium Sulfacetamide 9.8%, Sulfur 4.8%	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	3/27/2017	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Bi-Coastal Pharma International LLC	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