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BLEPHAMIDE
BLEPHAMIDE - 11980-022-10 - (sulfacetamide sodium and prednisolone acetate)
Drug Information of BLEPHAMIDE
| Product NDC: | 11980-022 |
| Proprietary Name: | BLEPHAMIDE |
| Non Proprietary Name: | sulfacetamide sodium and prednisolone acetate |
| Active Ingredient(s): | 2; 100 mg/mL; mg/mL & nbsp; sulfacetamide sodium and prednisolone acetate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SUSPENSION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BLEPHAMIDE
| Product NDC: | 11980-022 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA012813 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19611001 |
Package Information of BLEPHAMIDE
| Package NDC: | 11980-022-10 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (11980-022-10) > 10 mL in 1 BOTTLE, DROPPER |
NDC Information of BLEPHAMIDE
| NDC Code | 11980-022-10 |
| Proprietary Name | BLEPHAMIDE |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (11980-022-10) > 10 mL in 1 BOTTLE, DROPPER |
| Product NDC | 11980-022 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sulfacetamide sodium and prednisolone acetate |
| Dosage Form Name | SUSPENSION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19611001 |
| Marketing Category Name | NDA |
| Labeler Name | Allergan, Inc. |
| Substance Name | PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM |
| Strength Number | 2; 100 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
