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Dynarex Antifungal
Dynarex Antifungal - 67777-231-02 - (antifungal)
Drug Information of Dynarex Antifungal
| Product NDC: | 67777-231 |
| Proprietary Name: | Dynarex Antifungal |
| Non Proprietary Name: | antifungal |
| Active Ingredient(s): | 1 g/100g & nbsp; antifungal |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dynarex Antifungal
| Product NDC: | 67777-231 |
| Labeler Name: | Dynarex Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100518 |
Package Information of Dynarex Antifungal
| Package NDC: | 67777-231-02 |
| Package Description: | 28.25 g in 1 TUBE (67777-231-02) |
NDC Information of Dynarex Antifungal
| NDC Code | 67777-231-02 |
| Proprietary Name | Dynarex Antifungal |
| Package Description | 28.25 g in 1 TUBE (67777-231-02) |
| Product NDC | 67777-231 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | antifungal |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100518 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dynarex Corporation |
| Substance Name | CLOTRIMAZOLE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
