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Neomycin Sulfate - 0904-5941-06 - (Neomycin Sulfate)

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Drug Information of Neomycin Sulfate

Product NDC: 0904-5941
Proprietary Name: Neomycin Sulfate
Non Proprietary Name: Neomycin Sulfate
Active Ingredient(s): 500    mg/1 & nbsp;   Neomycin Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Neomycin Sulfate

Product NDC: 0904-5941
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA060304
Marketing Category: ANDA
Start Marketing Date: 20090914

Package Information of Neomycin Sulfate

Package NDC: 0904-5941-06
Package Description: 50 TABLET in 1 BOX, UNIT-DOSE (0904-5941-06)

NDC Information of Neomycin Sulfate

NDC Code 0904-5941-06
Proprietary Name Neomycin Sulfate
Package Description 50 TABLET in 1 BOX, UNIT-DOSE (0904-5941-06)
Product NDC 0904-5941
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Neomycin Sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090914
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name NEOMYCIN SULFATE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of Neomycin Sulfate


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