Product NDC: | 0363-0737 |
Proprietary Name: | Miconazole 1 |
Non Proprietary Name: | Miconazole nitrate |
Active Ingredient(s): | & nbsp; Miconazole nitrate |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0363-0737 |
Labeler Name: | Walgreen Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA079114 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100608 |
Package NDC: | 0363-0737-45 |
Package Description: | 1 KIT in 1 CARTON (0363-0737-45) * 9 g in 1 TUBE * 1 SWAB in 1 PACKAGE * 1 INSERT in 1 BLISTER PACK |
NDC Code | 0363-0737-45 |
Proprietary Name | Miconazole 1 |
Package Description | 1 KIT in 1 CARTON (0363-0737-45) * 9 g in 1 TUBE * 1 SWAB in 1 PACKAGE * 1 INSERT in 1 BLISTER PACK |
Product NDC | 0363-0737 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Miconazole nitrate |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20100608 |
Marketing Category Name | ANDA |
Labeler Name | Walgreen Company |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |