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bacitracin
bacitracin - 37808-536-64 - (Bacitracin)
Drug Information of bacitracin
| Product NDC: | 37808-536 |
| 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) |
Labeler Information of bacitracin
| Product NDC: | 37808-536 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19910615 |
Package Information of bacitracin
| Package NDC: | 37808-536-64 |
| Package Description: | 1 TUBE in 1 CARTON (37808-536-64) > 28 g in 1 TUBE |
NDC Information of bacitracin
| NDC Code | 37808-536-64 |
| Proprietary Name | bacitracin |
| Package Description | 1 TUBE in 1 CARTON (37808-536-64) > 28 g in 1 TUBE |
| Product NDC | 37808-536 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bacitracin |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19910615 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | H E B |
| Substance Name | BACITRACIN |
| Strength Number | 500 |
| Strength Unit | [USP'U]/g |
| Pharmaceutical Classes |
