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] |