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SULFACETAMIDE SODIUM
SULFACETAMIDE SODIUM - 48102-103-35 - (SULFACETAMIDE SODIUM)
Drug Information of SULFACETAMIDE SODIUM
| Product NDC: | 48102-103 |
| Proprietary Name: | SULFACETAMIDE SODIUM |
| Non Proprietary Name: | SULFACETAMIDE SODIUM |
| Active Ingredient(s): | 100 mg/g & nbsp; SULFACETAMIDE SODIUM |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SULFACETAMIDE SODIUM
| Product NDC: | 48102-103 |
| Labeler Name: | Fera Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080029 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120301 |
Package Information of SULFACETAMIDE SODIUM
| Package NDC: | 48102-103-35 |
| Package Description: | 1 TUBE in 1 CARTON (48102-103-35) > 3.5 g in 1 TUBE |
NDC Information of SULFACETAMIDE SODIUM
| NDC Code | 48102-103-35 |
| Proprietary Name | SULFACETAMIDE SODIUM |
| Package Description | 1 TUBE in 1 CARTON (48102-103-35) > 3.5 g in 1 TUBE |
| Product NDC | 48102-103 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SULFACETAMIDE SODIUM |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20120301 |
| Marketing Category Name | ANDA |
| Labeler Name | Fera Pharmaceuticals, LLC |
| Substance Name | SULFACETAMIDE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
