Product NDC: | 59779-536 |
Proprietary Name: | BACITRACIN |
Non Proprietary Name: | Bacitracin |
Active Ingredient(s): | 500 [USP'U]/g & nbsp; Bacitracin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-536 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20050608 |
Package NDC: | 59779-536-64 |
Package Description: | 1 TUBE in 1 CARTON (59779-536-64) > 28 g in 1 TUBE |
NDC Code | 59779-536-64 |
Proprietary Name | BACITRACIN |
Package Description | 1 TUBE in 1 CARTON (59779-536-64) > 28 g in 1 TUBE |
Product NDC | 59779-536 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Bacitracin |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20050608 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CVS Pharmacy |
Substance Name | BACITRACIN |
Strength Number | 500 |
Strength Unit | [USP'U]/g |
Pharmaceutical Classes |