Home
>
National Drug Code (NDC)
>
Claris
Claris - 58980-335-90 - (SULFACETAMIDE SODIUM and SULFUR)
Drug Information of Claris
| Product NDC: | 58980-335 |
| Proprietary Name: | Claris |
| Non Proprietary Name: | SULFACETAMIDE SODIUM and SULFUR |
| Active Ingredient(s): | 100; 40 mg/mL; mg/mL & nbsp; SULFACETAMIDE SODIUM and SULFUR |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Claris
| Product NDC: | 58980-335 |
| Labeler Name: | Stratus Pharamceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20090216 |
Package Information of Claris
| Package NDC: | 58980-335-90 |
| Package Description: | 1 BOTTLE in 1 BOX (58980-335-90) > 473 mL in 1 BOTTLE |
NDC Information of Claris
| NDC Code | 58980-335-90 |
| Proprietary Name | Claris |
| Package Description | 1 BOTTLE in 1 BOX (58980-335-90) > 473 mL in 1 BOTTLE |
| Product NDC | 58980-335 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SULFACETAMIDE SODIUM and SULFUR |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090216 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | Stratus Pharamceuticals, Inc |
| Substance Name | SULFACETAMIDE SODIUM; SULFUR |
| Strength Number | 100; 40 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
