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NEOSPORIN G.U. - 61570-048-20 - (neomycin sulfate - polymyxin B sulfate)

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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]

Complete Information of NEOSPORIN G.U.


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