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Bacitracin
Bacitracin - 0713-0280-31 - (Bacitracin)
Drug Information of Bacitracin
| Product NDC: | 0713-0280 |
| 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: | 0713-0280 |
| Labeler Name: | G&W Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19950110 |
Package Information of Bacitracin
| Package NDC: | 0713-0280-31 |
| Package Description: | 28.4 g in 1 TUBE (0713-0280-31) |
NDC Information of Bacitracin
| NDC Code | 0713-0280-31 |
| Proprietary Name | Bacitracin |
| Package Description | 28.4 g in 1 TUBE (0713-0280-31) |
| Product NDC | 0713-0280 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bacitracin |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19950110 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | G&W Laboratories, Inc. |
| Substance Name | BACITRACIN |
| Strength Number | 500 |
| Strength Unit | [USP'U]/g |
| Pharmaceutical Classes |
