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] |