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Sulfacetamide Sodium - 52125-424-01 - (sulfacetamide sodium)

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Drug Information of Sulfacetamide Sodium

Product NDC: 52125-424
Proprietary Name: Sulfacetamide Sodium
Non Proprietary Name: sulfacetamide sodium
Active Ingredient(s): 100    mg/mL & nbsp;   sulfacetamide sodium
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Sulfacetamide Sodium

Product NDC: 52125-424
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040066
Marketing Category: ANDA
Start Marketing Date: 20130613

Package Information of Sulfacetamide Sodium

Package NDC: 52125-424-01
Package Description: 15 mL in 1 BOTTLE, DROPPER (52125-424-01)

NDC Information of Sulfacetamide Sodium

NDC Code 52125-424-01
Proprietary Name Sulfacetamide Sodium
Package Description 15 mL in 1 BOTTLE, DROPPER (52125-424-01)
Product NDC 52125-424
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sulfacetamide sodium
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20130613
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name SULFACETAMIDE SODIUM
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient]

Complete Information of Sulfacetamide Sodium


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