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Sodium Sulfacetamide and Sulfur - 42192-133-16 - (Sodium Sulfacetamide and Sulfur)

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Drug Information of Sodium Sulfacetamide and Sulfur

Product NDC: 42192-133
Proprietary Name: Sodium Sulfacetamide and Sulfur
Non Proprietary Name: Sodium Sulfacetamide and Sulfur
Active Ingredient(s): 80; 40    mg/mL; mg/mL & nbsp;   Sodium Sulfacetamide and Sulfur
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Sulfacetamide and Sulfur

Product NDC: 42192-133
Labeler Name: Acella Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110727

Package Information of Sodium Sulfacetamide and Sulfur

Package NDC: 42192-133-16
Package Description: 473 mL in 1 BOTTLE (42192-133-16)

NDC Information of Sodium Sulfacetamide and Sulfur

NDC Code 42192-133-16
Proprietary Name Sodium Sulfacetamide and Sulfur
Package Description 473 mL in 1 BOTTLE (42192-133-16)
Product NDC 42192-133
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Sulfacetamide and Sulfur
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20110727
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Acella Pharmaceuticals, LLC
Substance Name SULFACETAMIDE SODIUM; SULFUR
Strength Number 80; 40
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient]

Complete Information of Sodium Sulfacetamide and Sulfur


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