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NEOMYCIN SULFATE - 60429-239-01 - (NEOMYCIN SULFATE)

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Drug Information of NEOMYCIN SULFATE

Product NDC: 60429-239
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: 60429-239
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065468
Marketing Category: ANDA
Start Marketing Date: 20110103

Package Information of NEOMYCIN SULFATE

Package NDC: 60429-239-01
Package Description: 100 TABLET in 1 BOTTLE (60429-239-01)

NDC Information of NEOMYCIN SULFATE

NDC Code 60429-239-01
Proprietary Name NEOMYCIN SULFATE
Package Description 100 TABLET in 1 BOTTLE (60429-239-01)
Product NDC 60429-239
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NEOMYCIN SULFATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110103
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
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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