NDC Code | 21695-736-35 |
Package Description | 3.5 g in 1 TUBE (21695-736-35) |
Product NDC | 21695-736 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Neomycin And Polymyxin B Sulfates And Bacitracin Zinc With Hydrocortisone Acetate |
Non-Proprietary Name | Neomycin Sulfate And Polymyxin B Sulfate, Bacitracin Zinc And Hydrocortisone Acetate |
Dosage Form | OINTMENT |
Usage | OPHTHALMIC |
Start Marketing Date | 19810414 |
Marketing Category Name | ANDA |
Application Number | ANDA062166 |
Manufacturer | Rebel Distributors Corp |
Substance Name | NEOMYCIN SULFATE; POLYMYXIN B SULFATE; BACITRACIN ZINC; HYDROCORTISONE ACETATE |
Strength | 3.5; 10000; 400; 10 |
Strength Unit | mg/g; g/g; g/g; mg/g |
Pharmacy 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] |