Product NDC: | 0904-2728 |
Proprietary Name: | Sulfacetamide Sodium |
Non Proprietary Name: | Sulfaccetamide Sodium |
Active Ingredient(s): | 100 mg/mL & nbsp; Sulfaccetamide Sodium |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0904-2728 |
Labeler Name: | Major Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040066 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040701 |
Package NDC: | 0904-2728-35 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0904-2728-35) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 0904-2728-35 |
Proprietary Name | Sulfacetamide Sodium |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0904-2728-35) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 0904-2728 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sulfaccetamide Sodium |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20040701 |
Marketing Category Name | ANDA |
Labeler Name | Major Pharmaceuticals |
Substance Name | SULFACETAMIDE SODIUM |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |