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Sulfacetamide Sodium
Sulfacetamide Sodium - 24208-670-04 - (sulfacetamide sodium)
Drug Information of Sulfacetamide Sodium
| Product NDC: | 24208-670 |
| 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) |
Labeler Information of Sulfacetamide Sodium
| Product NDC: | 24208-670 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040066 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19941228 |
Package Information of Sulfacetamide Sodium
| Package NDC: | 24208-670-04 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-670-04) > 15 mL in 1 BOTTLE, DROPPER |
NDC Information of Sulfacetamide Sodium
| NDC Code | 24208-670-04 |
| Proprietary Name | Sulfacetamide Sodium |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-670-04) > 15 mL in 1 BOTTLE, DROPPER |
| Product NDC | 24208-670 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sulfacetamide sodium |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19941228 |
| Marketing Category Name | ANDA |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | SULFACETAMIDE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
