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Carrington Antifungal
Carrington Antifungal - 53329-079-64 - (Miconazole Nitrate)
Drug Information of Carrington Antifungal
| Product NDC: | 53329-079 |
| Proprietary Name: | Carrington Antifungal |
| Non Proprietary Name: | Miconazole Nitrate |
| Active Ingredient(s): | 20 mg/g & nbsp; Miconazole Nitrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Carrington Antifungal
| Product NDC: | 53329-079 |
| Labeler Name: | Medline Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20070101 |
Package Information of Carrington Antifungal
| Package NDC: | 53329-079-64 |
| Package Description: | 141 g in 1 TUBE (53329-079-64) |
NDC Information of Carrington Antifungal
| NDC Code | 53329-079-64 |
| Proprietary Name | Carrington Antifungal |
| Package Description | 141 g in 1 TUBE (53329-079-64) |
| Product NDC | 53329-079 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole Nitrate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20070101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Medline Industries, Inc. |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
