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Sulfacetamide Sodium and Prednisolone Sodium Phosphate - 61314-297-05 - (Sulfacetamide Sodium and Prednisolone Sodium Phosphate)

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Drug Information of Sulfacetamide Sodium and Prednisolone Sodium Phosphate

Product NDC: 61314-297
Proprietary Name: Sulfacetamide Sodium and Prednisolone Sodium Phosphate
Non Proprietary Name: Sulfacetamide Sodium and Prednisolone Sodium Phosphate
Active Ingredient(s): 2.5; 100    mg/mL; mg/mL & nbsp;   Sulfacetamide Sodium and Prednisolone Sodium Phosphate
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sulfacetamide Sodium and Prednisolone Sodium Phosphate

Product NDC: 61314-297
Labeler Name: Falcon Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073630
Marketing Category: ANDA
Start Marketing Date: 20040309

Package Information of Sulfacetamide Sodium and Prednisolone Sodium Phosphate

Package NDC: 61314-297-05
Package Description: 5 mL in 1 BOTTLE (61314-297-05)

NDC Information of Sulfacetamide Sodium and Prednisolone Sodium Phosphate

NDC Code 61314-297-05
Proprietary Name Sulfacetamide Sodium and Prednisolone Sodium Phosphate
Package Description 5 mL in 1 BOTTLE (61314-297-05)
Product NDC 61314-297
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sulfacetamide Sodium and Prednisolone Sodium Phosphate
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20040309
Marketing Category Name ANDA
Labeler Name Falcon Pharmaceuticals, Ltd.
Substance Name PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM
Strength Number 2.5; 100
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Sulfacetamide Sodium and Prednisolone Sodium Phosphate


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