CORTISPORIN is a Topical Ointment in the Human Prescription Drug category. It is labeled and distributed by Pfizer Laboratories Div Pfizer Inc. The primary component is Neomycin Sulfate; Polymyxin B Sulfate; Bacitracin Zinc; Hydrocortisone.
Product ID | 61570-031_8304d7f0-2617-4a53-97fc-d32a93925f2f |
NDC | 61570-031 |
Product Type | Human Prescription Drug |
Proprietary Name | CORTISPORIN |
Generic Name | Neomycin And Polymyxin B Sulfates, Bacitracin Zinc, And Hydrocortisone |
Dosage Form | Ointment |
Route of Administration | TOPICAL |
Marketing Start Date | 1955-04-15 |
Marketing Category | NDA / NDA |
Application Number | NDA050168 |
Labeler Name | Pfizer Laboratories Div Pfizer Inc |
Substance Name | NEOMYCIN SULFATE; POLYMYXIN B SULFATE; BACITRACIN ZINC; HYDROCORTISONE |
Active Ingredient Strength | 4 mg/g; [iU]/g; [iU]/g; mg/g |
Pharm Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [CS],Polymyxin-class Antibacterial [EPC],Polymyxins [CS],Decreased Cell Wall Synthesis & Repair [PE],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 1955-04-15 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA050168 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | GM |
Marketing Start Date | 1955-04-15 |
Ingredient | Strength |
---|---|
NEOMYCIN SULFATE | 3.5 mg/g |
SPL SET ID: | 097a7a8d-04d4-4736-c8b7-0796117457bf |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
61570-031 | CORTISPORIN | neomycin and polymyxin B sulfates, bacitracin zinc, and hydrocortisone |
61570-032 | CORTISPORIN | neomycin sulfate, polymyxin B sulfate, and hydrocortisone acetate |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CORTISPORIN 71677134 0616775 Live/Registered |
BURROUGHS WELLCOME & CO. (U. S. A.) INC. 1954-11-23 |