Home > National Drug Code (NDC) > Neomycin Sulfate

Neomycin Sulfate - 50383-565-10 - (Neomycin Sulfate)

Alphabetical Index


Drug Information of Neomycin Sulfate

Product NDC: 50383-565
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: 50383-565
Labeler Name: HI TECH PHARMACAL CO INC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065220
Marketing Category: ANDA
Start Marketing Date: 20100312

Package Information of Neomycin Sulfate

Package NDC: 50383-565-10
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (50383-565-10)

NDC Information of Neomycin Sulfate

NDC Code 50383-565-10
Proprietary Name Neomycin Sulfate
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (50383-565-10)
Product NDC 50383-565
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Neomycin Sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100312
Marketing Category Name ANDA
Labeler Name HI TECH PHARMACAL CO 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


General Information