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NEOSPORIN G.U.
NEOSPORIN G.U. - 61570-048-20 - (neomycin sulfate - polymyxin B sulfate)
Drug Information of NEOSPORIN G.U.
| Product NDC: | 61570-048 |
| Proprietary Name: | NEOSPORIN G.U. |
| Non Proprietary Name: | neomycin sulfate - polymyxin B sulfate |
| Active Ingredient(s): | 40; 200000 mg/mL; [iU]/mL & nbsp; neomycin sulfate - polymyxin B sulfate |
| Administration Route(s): | IRRIGATION |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NEOSPORIN G.U.
| Product NDC: | 61570-048 |
| Labeler Name: | Monarch Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA060707 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19660628 |
Package Information of NEOSPORIN G.U.
| Package NDC: | 61570-048-20 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (61570-048-20) > 20 mL in 1 VIAL, MULTI-DOSE |
NDC Information of NEOSPORIN G.U.
| NDC Code | 61570-048-20 |
| Proprietary Name | NEOSPORIN G.U. |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (61570-048-20) > 20 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 61570-048 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | neomycin sulfate - polymyxin B sulfate |
| Dosage Form Name | SOLUTION |
| Route Name | IRRIGATION |
| Start Marketing Date | 19660628 |
| Marketing Category Name | ANDA |
| Labeler Name | Monarch Pharmaceuticals, Inc. |
| Substance Name | NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
| Strength Number | 40; 200000 |
| Strength Unit | mg/mL; [iU]/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient] |
