Product NDC: | 51141-0066 |
Proprietary Name: | Antibiotic Ointment |
Non Proprietary Name: | Neomycin Sulfate |
Active Ingredient(s): | 3.5 mg/g & nbsp; Neomycin Sulfate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51141-0066 |
Labeler Name: | NeoPharm Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100826 |
Package NDC: | 51141-0066-1 |
Package Description: | 1 TUBE in 1 BOX (51141-0066-1) > 28 g in 1 TUBE |
NDC Code | 51141-0066-1 |
Proprietary Name | Antibiotic Ointment |
Package Description | 1 TUBE in 1 BOX (51141-0066-1) > 28 g in 1 TUBE |
Product NDC | 51141-0066 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Neomycin Sulfate |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20100826 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | NeoPharm Co., Ltd. |
Substance Name | NEOMYCIN SULFATE |
Strength Number | 3.5 |
Strength Unit | mg/g |
Pharmaceutical Classes |