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Sulfacetamide Sodium - 61314-701-01 - (Sulfacetamide Sodium)

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Drug Information of Sulfacetamide Sodium

Product NDC: 61314-701
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
Coding System: National Drug Codes(NDC)

Labeler Information of Sulfacetamide Sodium

Product NDC: 61314-701
Labeler Name: Falcon Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089560
Marketing Category: ANDA
Start Marketing Date: 20030325

Package Information of Sulfacetamide Sodium

Package NDC: 61314-701-01
Package Description: 15 mL in 1 BOTTLE, PLASTIC (61314-701-01)

NDC Information of Sulfacetamide Sodium

NDC Code 61314-701-01
Proprietary Name Sulfacetamide Sodium
Package Description 15 mL in 1 BOTTLE, PLASTIC (61314-701-01)
Product NDC 61314-701
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sulfacetamide Sodium
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20030325
Marketing Category Name ANDA
Labeler Name Falcon Pharmaceuticals, Ltd.
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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