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Sulfacetamide Sodium and Prednisolone Sodium Phosphate - 24208-317-10 - (Sulfacetamide Sodium and Prednisolone Sodium Phosphate)

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Drug Information of Sulfacetamide Sodium and Prednisolone Sodium Phosphate

Product NDC: 24208-317
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/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Sulfacetamide Sodium and Prednisolone Sodium Phosphate

Product NDC: 24208-317
Labeler Name: Bausch & Lomb Incoporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074449
Marketing Category: ANDA
Start Marketing Date: 19951229

Package Information of Sulfacetamide Sodium and Prednisolone Sodium Phosphate

Package NDC: 24208-317-10
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (24208-317-10) > 10 mL in 1 BOTTLE, DROPPER

NDC Information of Sulfacetamide Sodium and Prednisolone Sodium Phosphate

NDC Code 24208-317-10
Proprietary Name Sulfacetamide Sodium and Prednisolone Sodium Phosphate
Package Description 1 BOTTLE, DROPPER in 1 CARTON (24208-317-10) > 10 mL in 1 BOTTLE, DROPPER
Product NDC 24208-317
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sulfacetamide Sodium and Prednisolone Sodium Phosphate
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19951229
Marketing Category Name ANDA
Labeler Name Bausch & Lomb Incoporated
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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