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Sulfacetamide Sodium - 49999-144-15 - (sulfacetamide sodium)

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Drug Information of Sulfacetamide Sodium

Product NDC: 49999-144
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: 49999-144
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040066
Marketing Category: ANDA
Start Marketing Date: 19941228

Package Information of Sulfacetamide Sodium

Package NDC: 49999-144-15
Package Description: 15 mL in 1 BOTTLE, PLASTIC (49999-144-15)

NDC Information of Sulfacetamide Sodium

NDC Code 49999-144-15
Proprietary Name Sulfacetamide Sodium
Package Description 15 mL in 1 BOTTLE, PLASTIC (49999-144-15)
Product NDC 49999-144
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sulfacetamide sodium
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19941228
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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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