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Neocidin
Neocidin - 0904-3016-10 - (Neomycin and Polymyxin B Sulfates and Gramicidin)
Drug Information of Neocidin
| Product NDC: | 0904-3016 |
| Proprietary Name: | Neocidin |
| Non Proprietary Name: | Neomycin and Polymyxin B Sulfates and Gramicidin |
| Active Ingredient(s): | .025; 1.75; 10000 mg/mL; mg/mL; [USP'U]/mL & nbsp; Neomycin and Polymyxin B Sulfates and Gramicidin |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neocidin
| Product NDC: | 0904-3016 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064047 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040607 |
Package Information of Neocidin
| Package NDC: | 0904-3016-10 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0904-3016-10) > 10 mL in 1 BOTTLE, DROPPER |
NDC Information of Neocidin
| NDC Code | 0904-3016-10 |
| Proprietary Name | Neocidin |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0904-3016-10) > 10 mL in 1 BOTTLE, DROPPER |
| Product NDC | 0904-3016 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Neomycin and Polymyxin B Sulfates and Gramicidin |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20040607 |
| Marketing Category Name | ANDA |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | GRAMICIDIN; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
| Strength Number | .025; 1.75; 10000 |
| Strength Unit | mg/mL; mg/mL; [USP'U]/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient] |
