Product NDC: | 11822-0982 |
Proprietary Name: | Miconazole 3 |
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: | 11822-0982 |
Labeler Name: | Rite Aid Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA076357 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060818 |
Package NDC: | 11822-0982-0 |
Package Description: | 1 KIT in 1 CARTON (11822-0982-0) * 1 APPLICATOR in 1 POUCH > 5 g in 1 APPLICATOR * 9 g in 1 TUBE * 2 POUCH in 1 PACKAGE > 3 SWAB in 1 POUCH |
NDC Code | 11822-0982-0 |
Proprietary Name | Miconazole 3 |
Package Description | 1 KIT in 1 CARTON (11822-0982-0) * 1 APPLICATOR in 1 POUCH > 5 g in 1 APPLICATOR * 9 g in 1 TUBE * 2 POUCH in 1 PACKAGE > 3 SWAB in 1 POUCH |
Product NDC | 11822-0982 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | miconazole nitrate |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20060818 |
Marketing Category Name | ANDA |
Labeler Name | Rite Aid Corporation |
Substance Name | |
Strength Number | |
Strength Unit | |
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