Product NDC: | 54868-1157 |
Proprietary Name: | BLEPHAMIDE |
Non Proprietary Name: | sulfacetamide sodium and prednisolone acetate |
Active Ingredient(s): | 2; 100 mg/g; mg/g & nbsp; sulfacetamide sodium and prednisolone acetate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-1157 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA087748 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120304 |
Package NDC: | 54868-1157-0 |
Package Description: | 1 TUBE in 1 CARTON (54868-1157-0) > 3.5 g in 1 TUBE |
NDC Code | 54868-1157-0 |
Proprietary Name | BLEPHAMIDE |
Package Description | 1 TUBE in 1 CARTON (54868-1157-0) > 3.5 g in 1 TUBE |
Product NDC | 54868-1157 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sulfacetamide sodium and prednisolone acetate |
Dosage Form Name | OINTMENT |
Route Name | OPHTHALMIC |
Start Marketing Date | 20120304 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM |
Strength Number | 2; 100 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |