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Triple Antibiotic
Triple Antibiotic - 55154-0156-5 - (Neomycin, Polymyxin B Sulfates, Bacitracin)
Drug Information of Triple Antibiotic
| Product NDC: | 55154-0156 |
| Proprietary Name: | Triple Antibiotic |
| Non Proprietary Name: | Neomycin, Polymyxin B Sulfates, Bacitracin |
| Active Ingredient(s): | 400; 3.5; 5000 [USP'U]/1; mg/1; [USP'U]/1 & nbsp; Neomycin, Polymyxin B Sulfates, Bacitracin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Triple Antibiotic
| Product NDC: | 55154-0156 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110606 |
Package Information of Triple Antibiotic
| Package NDC: | 55154-0156-5 |
| Package Description: | 6 PACKET in 1 BLISTER PACK (55154-0156-5) > 1 OINTMENT in 1 PACKET |
NDC Information of Triple Antibiotic
| NDC Code | 55154-0156-5 |
| Proprietary Name | Triple Antibiotic |
| Package Description | 6 PACKET in 1 BLISTER PACK (55154-0156-5) > 1 OINTMENT in 1 PACKET |
| Product NDC | 55154-0156 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Neomycin, Polymyxin B Sulfates, Bacitracin |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110606 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cardinal Health |
| Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
| Strength Number | 400; 3.5; 5000 |
| Strength Unit | [USP'U]/1; mg/1; [USP'U]/1 |
| Pharmaceutical Classes |
