Product NDC: | 68169-0022 |
Proprietary Name: | SHOPKO TRIPLE ANTIBIOTIC |
Non Proprietary Name: | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATE |
Active Ingredient(s): | 400; 3.5; 5000 [iU]/g; mg/g; [iU]/g & nbsp; BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68169-0022 |
Labeler Name: | TAI GUK PHARM. CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101220 |
Package NDC: | 68169-0022-8 |
Package Description: | 1 TUBE in 1 CARTON (68169-0022-8) > 28 g in 1 TUBE |
NDC Code | 68169-0022-8 |
Proprietary Name | SHOPKO TRIPLE ANTIBIOTIC |
Package Description | 1 TUBE in 1 CARTON (68169-0022-8) > 28 g in 1 TUBE |
Product NDC | 68169-0022 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATE |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20101220 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | TAI GUK PHARM. CO., LTD. |
Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
Strength Number | 400; 3.5; 5000 |
Strength Unit | [iU]/g; mg/g; [iU]/g |
Pharmaceutical Classes |