Product NDC: | 16590-209 |
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/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-209 |
Labeler Name: | STAT RX USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA089560 |
Marketing Category: | ANDA |
Start Marketing Date: | 19881018 |
Package NDC: | 16590-209-15 |
Package Description: | 15 mL in 1 BOTTLE, PLASTIC (16590-209-15) |
NDC Code | 16590-209-15 |
Proprietary Name | SULFACETAMIDE SODIUM |
Package Description | 15 mL in 1 BOTTLE, PLASTIC (16590-209-15) |
Product NDC | 16590-209 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SULFACETAMIDE SODIUM |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 19881018 |
Marketing Category Name | ANDA |
Labeler Name | STAT RX USA LLC |
Substance Name | SULFACETAMIDE SODIUM |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |