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Bacitracin
Bacitracin - 67777-219-01 - (Bacitracin)
Drug Information of Bacitracin
| Product NDC: | 67777-219 |
| Proprietary Name: | Bacitracin |
| Non Proprietary Name: | Bacitracin |
| Active Ingredient(s): | 500 [iU]/g & nbsp; Bacitracin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bacitracin
| Product NDC: | 67777-219 |
| Labeler Name: | Dynarex Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091201 |
Package Information of Bacitracin
| Package NDC: | 67777-219-01 |
| Package Description: | 72 TUBE in 1 CASE (67777-219-01) > 28.35 g in 1 TUBE |
NDC Information of Bacitracin
| NDC Code | 67777-219-01 |
| Proprietary Name | Bacitracin |
| Package Description | 72 TUBE in 1 CASE (67777-219-01) > 28.35 g in 1 TUBE |
| Product NDC | 67777-219 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bacitracin |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20091201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dynarex Corporation |
| Substance Name | BACITRACIN |
| Strength Number | 500 |
| Strength Unit | [iU]/g |
| Pharmaceutical Classes |
