| 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] |