| Product NDC: | 11980-011 |
| Proprietary Name: | BLEPH-10 |
| 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: | 11980-011 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA080028 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19710601 |
| Package NDC: | 11980-011-05 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (11980-011-05) > 5 mL in 1 BOTTLE, PLASTIC |
| NDC Code | 11980-011-05 |
| Proprietary Name | BLEPH-10 |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (11980-011-05) > 5 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 11980-011 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sulfacetamide sodium |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19710601 |
| Marketing Category Name | NDA |
| Labeler Name | Allergan, Inc. |
| Substance Name | SULFACETAMIDE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |