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