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AK-POLY-BAC
AK-POLY-BAC - 17478-238-35 - (Bacitracin Zinc and Polymyxin B Sulfate)
Drug Information of AK-POLY-BAC
| Product NDC: | 17478-238 |
| Proprietary Name: | AK-POLY-BAC |
| Non Proprietary Name: | Bacitracin Zinc and Polymyxin B Sulfate |
| Active Ingredient(s): | 500; 10000 [USP'U]/g; [USP'U]/g & nbsp; Bacitracin Zinc and Polymyxin B Sulfate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AK-POLY-BAC
| Product NDC: | 17478-238 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064028 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060508 |
Package Information of AK-POLY-BAC
| Package NDC: | 17478-238-35 |
| Package Description: | 1 TUBE in 1 CARTON (17478-238-35) > 3.5 g in 1 TUBE |
NDC Information of AK-POLY-BAC
| NDC Code | 17478-238-35 |
| Proprietary Name | AK-POLY-BAC |
| Package Description | 1 TUBE in 1 CARTON (17478-238-35) > 3.5 g in 1 TUBE |
| Product NDC | 17478-238 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Bacitracin Zinc and Polymyxin B Sulfate |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20060508 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn, Inc. |
| Substance Name | BACITRACIN ZINC; POLYMYXIN B SULFATE |
| Strength Number | 500; 10000 |
| Strength Unit | [USP'U]/g; [USP'U]/g |
| Pharmaceutical Classes | Decreased Cell Wall Synthesis & Repair [PE],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient] |
