Product NDC: | 11822-0199 |
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: | 11822-0199 |
Labeler Name: | Rite Aid Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA079114 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100609 |
Package NDC: | 11822-0199-0 |
Package Description: | 1 KIT in 1 CARTON (11822-0199-0) * 1 INSERT in 1 BLISTER PACK * 9 g in 1 TUBE |
NDC Code | 11822-0199-0 |
Proprietary Name | miconazole 1 |
Package Description | 1 KIT in 1 CARTON (11822-0199-0) * 1 INSERT in 1 BLISTER PACK * 9 g in 1 TUBE |
Product NDC | 11822-0199 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Miconazole nitrate |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20100609 |
Marketing Category Name | ANDA |
Labeler Name | Rite Aid Corporation |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |