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NEOCIDIN
NEOCIDIN - 0904-3012-38 - (Neomycin sulfate, Polymyxin B Sulfate and Bacitracin Zinc)
Drug Information of NEOCIDIN
| Product NDC: | 0904-3012 |
| Proprietary Name: | NEOCIDIN |
| 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 NEOCIDIN
| Product NDC: | 0904-3012 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064064 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19951030 |
Package Information of NEOCIDIN
| Package NDC: | 0904-3012-38 |
| Package Description: | 1 TUBE in 1 CARTON (0904-3012-38) > 3.5 g in 1 TUBE |
NDC Information of NEOCIDIN
| NDC Code | 0904-3012-38 |
| Proprietary Name | NEOCIDIN |
| Package Description | 1 TUBE in 1 CARTON (0904-3012-38) > 3.5 g in 1 TUBE |
| Product NDC | 0904-3012 |
| 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 | Major Pharmaceuticals |
| 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] |
