Product NDC: | 49348-274 |
Proprietary Name: | sunmark |
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): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49348-274 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120321 |
Package NDC: | 49348-274-72 |
Package Description: | 1 TUBE in 1 CARTON (49348-274-72) > 28.4 g in 1 TUBE |
NDC Code | 49348-274-72 |
Proprietary Name | sunmark |
Package Description | 1 TUBE in 1 CARTON (49348-274-72) > 28.4 g in 1 TUBE |
Product NDC | 49348-274 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Bacitracin zinc and Polymyxin B sulfate |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20120321 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | McKesson |
Substance Name | BACITRACIN ZINC; POLYMYXIN B SULFATE |
Strength Number | 500; 10000 |
Strength Unit | [USP'U]/g; [USP'U]/g |
Pharmaceutical Classes |