Product NDC: | 61314-701 |
Proprietary Name: | Sulfacetamide Sodium |
Non Proprietary Name: | Sulfacetamide Sodium |
Active Ingredient(s): | 100 mg/mL & nbsp; Sulfacetamide Sodium |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61314-701 |
Labeler Name: | Falcon Pharmaceuticals, Ltd. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA089560 |
Marketing Category: | ANDA |
Start Marketing Date: | 20030325 |
Package NDC: | 61314-701-01 |
Package Description: | 15 mL in 1 BOTTLE, PLASTIC (61314-701-01) |
NDC Code | 61314-701-01 |
Proprietary Name | Sulfacetamide Sodium |
Package Description | 15 mL in 1 BOTTLE, PLASTIC (61314-701-01) |
Product NDC | 61314-701 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sulfacetamide Sodium |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20030325 |
Marketing Category Name | ANDA |
Labeler Name | Falcon Pharmaceuticals, Ltd. |
Substance Name | SULFACETAMIDE SODIUM |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |