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Polymyxin B Sulfate and Trimethoprim
Polymyxin B Sulfate and Trimethoprim - 21695-335-10 - (polymyxin B sulfate and trimethoprim)
Drug Information of Polymyxin B Sulfate and Trimethoprim
| Product NDC: | 21695-335 |
| Proprietary Name: | Polymyxin B Sulfate and Trimethoprim |
| Non Proprietary Name: | polymyxin B sulfate and trimethoprim |
| Active Ingredient(s): | 10000; 1 mL/mL; mg/mL & nbsp; polymyxin B sulfate and trimethoprim |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Polymyxin B Sulfate and Trimethoprim
| Product NDC: | 21695-335 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064211 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19980413 |
Package Information of Polymyxin B Sulfate and Trimethoprim
| Package NDC: | 21695-335-10 |
| Package Description: | 10 mL in 1 BOTTLE, PLASTIC (21695-335-10) |
NDC Information of Polymyxin B Sulfate and Trimethoprim
| NDC Code | 21695-335-10 |
| Proprietary Name | Polymyxin B Sulfate and Trimethoprim |
| Package Description | 10 mL in 1 BOTTLE, PLASTIC (21695-335-10) |
| Product NDC | 21695-335 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | polymyxin B sulfate and trimethoprim |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19980413 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE |
| Strength Number | 10000; 1 |
| Strength Unit | mL/mL; mg/mL |
| Pharmaceutical Classes | Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient],Dihydrofolate Reductase Inhibitor Antibacterial [EPC],Dihydrofolate Reductase Inhibitors [MoA] |
