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Baza Antifungal
Baza Antifungal - 11701-045-23 - (Miconazole nitrate)
Drug Information of Baza Antifungal
| Product NDC: | 11701-045 |
| Proprietary Name: | Baza 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 Baza Antifungal
| Product NDC: | 11701-045 |
| Labeler Name: | Coloplast Manufacturing US, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090615 |
Package Information of Baza Antifungal
| Package NDC: | 11701-045-23 |
| Package Description: | 57 g in 1 TUBE (11701-045-23) |
NDC Information of Baza Antifungal
| NDC Code | 11701-045-23 |
| Proprietary Name | Baza Antifungal |
| Package Description | 57 g in 1 TUBE (11701-045-23) |
| Product NDC | 11701-045 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole nitrate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090615 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Coloplast Manufacturing US, LLC |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
