Home
>
National Drug Code (NDC)
>
Neomycin Sulfate
Neomycin Sulfate - 39822-0310-5 - (Neomycin Sulfate)
Drug Information of Neomycin Sulfate
| Product NDC: | 39822-0310 |
| 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: | 39822-0310 |
| Labeler Name: | X-GEN Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065220 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100312 |
Package Information of Neomycin Sulfate
| Package NDC: | 39822-0310-5 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (39822-0310-5) > 1 TABLET in 1 BLISTER PACK (39822-0310-7) |
NDC Information of Neomycin Sulfate
| NDC Code | 39822-0310-5 |
| Proprietary Name | Neomycin Sulfate |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (39822-0310-5) > 1 TABLET in 1 BLISTER PACK (39822-0310-7) |
| Product NDC | 39822-0310 |
| 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 | X-GEN Pharmaceuticals, Inc. |
| Substance Name | NEOMYCIN SULFATE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
