Neo-Fradin - 39822-0330-2 - (Neomycin Sulfate)

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Drug Information of Neo-Fradin

Product NDC: 39822-0330
Proprietary Name: Neo-Fradin
Non Proprietary Name: Neomycin Sulfate
Active Ingredient(s): 87.5    mg/5mL & nbsp;   Neomycin Sulfate
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Neo-Fradin

Product NDC: 39822-0330
Labeler Name: X-GEN Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065010
Marketing Category: ANDA
Start Marketing Date: 20020523

Package Information of Neo-Fradin

Package NDC: 39822-0330-2
Package Description: 59 mL in 1 BOTTLE (39822-0330-2)

NDC Information of Neo-Fradin

NDC Code 39822-0330-2
Proprietary Name Neo-Fradin
Package Description 59 mL in 1 BOTTLE (39822-0330-2)
Product NDC 39822-0330
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Neomycin Sulfate
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20020523
Marketing Category Name ANDA
Labeler Name X-GEN Pharmaceuticals, Inc.
Substance Name NEOMYCIN SULFATE
Strength Number 87.5
Strength Unit mg/5mL
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]

Complete Information of Neo-Fradin


General Information