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MITRAZOL
MITRAZOL - 0064-0650-01 - (MITRAZOL NITRATE)
Drug Information of MITRAZOL
| Product NDC: | 0064-0650 |
| Proprietary Name: | MITRAZOL |
| Non Proprietary Name: | MITRAZOL NITRATE |
| Active Ingredient(s): | .02 g/g & nbsp; MITRAZOL NITRATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MITRAZOL
| Product NDC: | 0064-0650 |
| Labeler Name: | HEALTHPOINT, LTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20011001 |
Package Information of MITRAZOL
| Package NDC: | 0064-0650-01 |
| Package Description: | 28 g in 1 BOTTLE, PLASTIC (0064-0650-01) |
NDC Information of MITRAZOL
| NDC Code | 0064-0650-01 |
| Proprietary Name | MITRAZOL |
| Package Description | 28 g in 1 BOTTLE, PLASTIC (0064-0650-01) |
| Product NDC | 0064-0650 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MITRAZOL NITRATE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20011001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | HEALTHPOINT, LTD |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | .02 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
