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Bacitracin
Bacitracin - 55154-5844-5 - (Bacitracin)
Drug Information of Bacitracin
| Product NDC: | 55154-5844 |
| Proprietary Name: | Bacitracin |
| Non Proprietary Name: | Bacitracin |
| Active Ingredient(s): | 500 1/1 & nbsp; Bacitracin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bacitracin
| Product NDC: | 55154-5844 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110602 |
Package Information of Bacitracin
| Package NDC: | 55154-5844-5 |
| Package Description: | 6 PACKET in 1 BAG (55154-5844-5) > 1 OINTMENT in 1 PACKET |
NDC Information of Bacitracin
| NDC Code | 55154-5844-5 |
| Proprietary Name | Bacitracin |
| Package Description | 6 PACKET in 1 BAG (55154-5844-5) > 1 OINTMENT in 1 PACKET |
| Product NDC | 55154-5844 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bacitracin |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110602 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cardinal Health |
| Substance Name | BACITRACIN |
| Strength Number | 500 |
| Strength Unit | 1/1 |
| Pharmaceutical Classes |
