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BF-MICOZO
BF-MICOZO - 10884-2265-2 - (Miconazole Nitrate)
Drug Information of BF-MICOZO
| Product NDC: | 10884-2265 |
| Proprietary Name: | BF-MICOZO |
| 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 BF-MICOZO
| Product NDC: | 10884-2265 |
| Labeler Name: | Bright Future Pharmaceuticals Factory |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110308 |
Package Information of BF-MICOZO
| Package NDC: | 10884-2265-2 |
| Package Description: | 1 TUBE in 1 BOX (10884-2265-2) > 15 g in 1 TUBE (10884-2265-1) |
NDC Information of BF-MICOZO
| NDC Code | 10884-2265-2 |
| Proprietary Name | BF-MICOZO |
| Package Description | 1 TUBE in 1 BOX (10884-2265-2) > 15 g in 1 TUBE (10884-2265-1) |
| Product NDC | 10884-2265 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole Nitrate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110308 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Bright Future Pharmaceuticals Factory |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
