BLEPHAMIDE - 54868-1157-0 - (sulfacetamide sodium and prednisolone acetate)

Alphabetical Index


Drug Information of BLEPHAMIDE

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)

Labeler Information of BLEPHAMIDE

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 Information of BLEPHAMIDE

Package NDC: 54868-1157-0
Package Description: 1 TUBE in 1 CARTON (54868-1157-0) > 3.5 g in 1 TUBE

NDC Information of BLEPHAMIDE

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]

Complete Information of BLEPHAMIDE


General Information