Product NDC: | 10849-002 |
Proprietary Name: | Terapie Anti-Fungal |
Non Proprietary Name: | MICONAZOLE NITRATE |
Active Ingredient(s): | 2 g/100g & nbsp; MICONAZOLE NITRATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10849-002 |
Labeler Name: | Armand Dupree Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20111104 |
Package NDC: | 10849-002-01 |
Package Description: | 1 TUBE in 1 CARTON (10849-002-01) > 60 g in 1 TUBE |
NDC Code | 10849-002-01 |
Proprietary Name | Terapie Anti-Fungal |
Package Description | 1 TUBE in 1 CARTON (10849-002-01) > 60 g in 1 TUBE |
Product NDC | 10849-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | MICONAZOLE NITRATE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20111104 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Armand Dupree Inc. |
Substance Name | MICONAZOLE NITRATE |
Strength Number | 2 |
Strength Unit | g/100g |
Pharmaceutical Classes |