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Miconazole Nitrate
Miconazole Nitrate - 0472-1736-07 - (miconazole nitrate)
Drug Information of Miconazole Nitrate
| Product NDC: | 0472-1736 |
| Proprietary Name: | Miconazole Nitrate |
| Non Proprietary Name: | miconazole nitrate |
| Active Ingredient(s): | 100 ug/1 & nbsp; miconazole nitrate |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Miconazole Nitrate
| Product NDC: | 0472-1736 |
| Labeler Name: | Actavis Mid Atlantic LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA073507 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19931119 |
Package Information of Miconazole Nitrate
| Package NDC: | 0472-1736-07 |
| Package Description: | 7 SUPPOSITORY in 1 BOX (0472-1736-07) |
NDC Information of Miconazole Nitrate
| NDC Code | 0472-1736-07 |
| Proprietary Name | Miconazole Nitrate |
| Package Description | 7 SUPPOSITORY in 1 BOX (0472-1736-07) |
| Product NDC | 0472-1736 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | miconazole nitrate |
| Dosage Form Name | SUPPOSITORY |
| Route Name | VAGINAL |
| Start Marketing Date | 19931119 |
| Marketing Category Name | ANDA |
| Labeler Name | Actavis Mid Atlantic LLC |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 100 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes |
