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CORTISPORIN
CORTISPORIN - 61570-034-10 - (neomycin sulfate, polymyxin B sulfate and hydrocortisone)
Drug Information of CORTISPORIN
| Product NDC: | 61570-034 |
| Proprietary Name: | CORTISPORIN |
| Non Proprietary Name: | neomycin sulfate, polymyxin B sulfate and hydrocortisone |
| Active Ingredient(s): | 10; 3.5; 10000 mg/mL; mg/mL; [iU]/mL & nbsp; neomycin sulfate, polymyxin B sulfate and hydrocortisone |
| Administration Route(s): | AURICULAR (OTIC) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CORTISPORIN
| Product NDC: | 61570-034 |
| Labeler Name: | Monarch Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050479 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19751117 |
Package Information of CORTISPORIN
| Package NDC: | 61570-034-10 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (61570-034-10) > 10 mL in 1 BOTTLE, DROPPER |
NDC Information of CORTISPORIN
| NDC Code | 61570-034-10 |
| Proprietary Name | CORTISPORIN |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (61570-034-10) > 10 mL in 1 BOTTLE, DROPPER |
| Product NDC | 61570-034 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | neomycin sulfate, polymyxin B sulfate and hydrocortisone |
| Dosage Form Name | SOLUTION |
| Route Name | AURICULAR (OTIC) |
| Start Marketing Date | 19751117 |
| Marketing Category Name | NDA |
| Labeler Name | Monarch Pharmaceuticals, Inc. |
| Substance Name | HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
| Strength Number | 10; 3.5; 10000 |
| Strength Unit | mg/mL; mg/mL; [iU]/mL |
| Pharmaceutical Classes | Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
