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Zeasorb
Zeasorb - 0145-1501-03 - (miconazole nitrate)
Drug Information of Zeasorb
| Product NDC: | 0145-1501 |
| Proprietary Name: | Zeasorb |
| Non Proprietary Name: | miconazole nitrate |
| Active Ingredient(s): | 20.6 mg/g & nbsp; miconazole nitrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zeasorb
| Product NDC: | 0145-1501 |
| Labeler Name: | Stiefel Laboratories Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110314 |
Package Information of Zeasorb
| Package NDC: | 0145-1501-03 |
| Package Description: | 71 g in 1 BOTTLE (0145-1501-03) |
NDC Information of Zeasorb
| NDC Code | 0145-1501-03 |
| Proprietary Name | Zeasorb |
| Package Description | 71 g in 1 BOTTLE (0145-1501-03) |
| Product NDC | 0145-1501 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | miconazole nitrate |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20110314 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Stiefel Laboratories Inc |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20.6 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
