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NEOSPORIN
NEOSPORIN - 61570-045-10 - (neomycin and polymyxin B sulfates and gramicidin)
Drug Information of NEOSPORIN
| Product NDC: | 61570-045 |
| Proprietary Name: | NEOSPORIN |
| Non Proprietary Name: | neomycin and polymyxin B sulfates and gramicidin |
| Active Ingredient(s): | .025; 1.75; 10000 mg/mL; mg/mL; [iU]/mL & nbsp; neomycin and polymyxin B sulfates and gramicidin |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NEOSPORIN
| Product NDC: | 61570-045 |
| Labeler Name: | Monarch Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA060582 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19550411 |
Package Information of NEOSPORIN
| Package NDC: | 61570-045-10 |
| Package Description: | 1 BOTTLE, DISPENSING in 1 CARTON (61570-045-10) > 10 mL in 1 BOTTLE, DISPENSING |
NDC Information of NEOSPORIN
| NDC Code | 61570-045-10 |
| Proprietary Name | NEOSPORIN |
| Package Description | 1 BOTTLE, DISPENSING in 1 CARTON (61570-045-10) > 10 mL in 1 BOTTLE, DISPENSING |
| Product NDC | 61570-045 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | neomycin and polymyxin B sulfates and gramicidin |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19550411 |
| Marketing Category Name | ANDA |
| Labeler Name | Monarch Pharmaceuticals, Inc. |
| Substance Name | GRAMICIDIN; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
| Strength Number | .025; 1.75; 10000 |
| Strength Unit | mg/mL; mg/mL; [iU]/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient] |
