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Triple Antibiotic
Triple Antibiotic - 57319-343-25 - (Neomycin sulfate, Polymyxin B Sulfate and Bacitracin Zinc)
Drug Information of Triple Antibiotic
| Product NDC: | 57319-343 |
| Proprietary Name: | Triple Antibiotic |
| Non Proprietary Name: | Neomycin sulfate, Polymyxin B Sulfate and Bacitracin Zinc |
| Active Ingredient(s): | 400; 3.5; 10000 [USP'U]/g; mg/g; [USP'U]/g & nbsp; Neomycin sulfate, Polymyxin B Sulfate and Bacitracin Zinc |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Triple Antibiotic
| Product NDC: | 57319-343 |
| Labeler Name: | Phoenix Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064064 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19951030 |
Package Information of Triple Antibiotic
| Package NDC: | 57319-343-25 |
| Package Description: | 1 TUBE in 1 CARTON (57319-343-25) > 3.5 g in 1 TUBE |
NDC Information of Triple Antibiotic
| NDC Code | 57319-343-25 |
| Proprietary Name | Triple Antibiotic |
| Package Description | 1 TUBE in 1 CARTON (57319-343-25) > 3.5 g in 1 TUBE |
| Product NDC | 57319-343 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Neomycin sulfate, Polymyxin B Sulfate and Bacitracin Zinc |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19951030 |
| Marketing Category Name | ANDA |
| Labeler Name | Phoenix Pharmaceutical, Inc. |
| Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
| Strength Number | 400; 3.5; 10000 |
| Strength Unit | [USP'U]/g; mg/g; [USP'U]/g |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient],Decreased Cell Wall Synthesis & Repair [PE] |
