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CORTISPORIN
CORTISPORIN - 61570-031-50 - (neomycin and polymyxin B sulfates, bacitracin zinc, and hydrocortisone)
Drug Information of CORTISPORIN
| Product NDC: | 61570-031 |
| Proprietary Name: | CORTISPORIN |
| Non Proprietary Name: | neomycin and polymyxin B sulfates, bacitracin zinc, and hydrocortisone |
| Active Ingredient(s): | 400; 10; 3.5; 5000 [iU]/g; mg/g; mg/g; [iU]/g & nbsp; neomycin and polymyxin B sulfates, bacitracin zinc, and hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CORTISPORIN
| Product NDC: | 61570-031 |
| Labeler Name: | Monarch Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050168 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19550415 |
Package Information of CORTISPORIN
| Package NDC: | 61570-031-50 |
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (61570-031-50) > 14.2 g in 1 TUBE, WITH APPLICATOR |
NDC Information of CORTISPORIN
| NDC Code | 61570-031-50 |
| Proprietary Name | CORTISPORIN |
| Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (61570-031-50) > 14.2 g in 1 TUBE, WITH APPLICATOR |
| Product NDC | 61570-031 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | neomycin and polymyxin B sulfates, bacitracin zinc, and hydrocortisone |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19550415 |
| Marketing Category Name | NDA |
| Labeler Name | Monarch Pharmaceuticals, Inc. |
| Substance Name | BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
| Strength Number | 400; 10; 3.5; 5000 |
| Strength Unit | [iU]/g; mg/g; mg/g; [iU]/g |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
