Product NDC: | 43288-250 |
Proprietary Name: | ORAVIG |
Non Proprietary Name: | miconazole |
Active Ingredient(s): | 50 mg/1 & nbsp; miconazole |
Administration Route(s): | BUCCAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43288-250 |
Labeler Name: | Praelia Pharmaceuticals Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022404 |
Marketing Category: | NDA |
Start Marketing Date: | 20121101 |
Package NDC: | 43288-250-14 |
Package Description: | 1 BOTTLE in 1 CARTON (43288-250-14) > 14 TABLET in 1 BOTTLE |
NDC Code | 43288-250-14 |
Proprietary Name | ORAVIG |
Package Description | 1 BOTTLE in 1 CARTON (43288-250-14) > 14 TABLET in 1 BOTTLE |
Product NDC | 43288-250 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | miconazole |
Dosage Form Name | TABLET |
Route Name | BUCCAL |
Start Marketing Date | 20121101 |
Marketing Category Name | NDA |
Labeler Name | Praelia Pharmaceuticals Inc |
Substance Name | MICONAZOLE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |